ENST00000264867.7:c.1318G>T
MANE Select
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ENSP00000264867.2:p.Ala440Ser
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ENST00000264867.6:c.1318G>T
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ENSP00000264867.2:p.Ala440Ser
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ENST00000506055.5:c.*533G>T
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ENSP00000423075.1:n.*533G>T
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ENST00000509702.5:n.1358G>T
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ENST00000613098.4:c.937G>T
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ENSP00000481498.1:p.Ala313Ser
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NM_013261.3:c.1318G>T
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NP_037393.1:p.Ala440Ser
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XM_005248130.2:c.1333G>T
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XP_005248187.1:p.Ala445Ser
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XM_005248131.3:c.1330G>T
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XP_005248188.1:p.Ala444Ser
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XM_005248132.1:c.1309G>T
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XP_005248189.1:p.Ala437Ser
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XM_005248134.3:c.1333G>T
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XP_005248191.1:p.Ala445Ser
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XM_011513764.1:c.1318G>T
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XP_011512066.1:p.Ala440Ser
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XM_011513765.1:c.1282G>T
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XP_011512067.1:p.Ala428Ser
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XM_011513766.1:c.1213G>T
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XP_011512068.1:p.Ala405Ser
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XM_011513767.1:c.1213G>T
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XP_011512069.1:p.Ala405Ser
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XM_011513768.1:c.1213G>T
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XP_011512070.1:p.Ala405Ser
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XM_011513769.1:c.1333G>T
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XP_011512071.1:p.Ala445Ser
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XM_011513770.1:c.937G>T
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XP_011512072.1:p.Ala313Ser
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XM_011513771.1:c.937G>T
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XP_011512073.1:p.Ala313Ser
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NM_001330751.1:c.1333G>T
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NP_001317680.1:p.Ala445Ser
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NM_001330752.1:c.1282G>T
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NP_001317681.1:p.Ala428Ser
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NM_001330753.1:c.937G>T
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NP_001317682.1:p.Ala313Ser
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NM_001354825.1:c.1333G>T
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NP_001341754.1:p.Ala445Ser
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NM_001354826.1:c.937G>T
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NP_001341755.1:p.Ala313Ser
|
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NM_001354827.1:c.1333G>T
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NP_001341756.1:p.Ala445Ser
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|
NM_013261.4:c.1318G>T
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NP_037393.1:p.Ala440Ser
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NR_148981.1:n.1845G>T
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NR_148982.1:n.1918G>T
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NR_148983.1:n.2071G>T
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NR_148984.1:n.1469G>T
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NR_148985.1:n.1983G>T
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NR_148986.1:n.1988G>T
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NR_148987.1:n.2070G>T
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XM_005248131.5:c.1330G>T
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XP_005248188.1:p.Ala444Ser
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XM_005248134.4:c.1333G>T
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XP_005248191.1:p.Ala445Ser
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XM_011513769.2:c.1333G>T
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XP_011512071.1:p.Ala445Ser
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XM_024453878.1:c.1333G>T
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XP_024309646.1:p.Ala445Ser
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NM_013261.5:c.1318G>T
MANE Select
|
NP_037393.1:p.Ala440Ser
|
|
NM_001330751.2:c.1333G>T
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NP_001317680.1:p.Ala445Ser
|
|
NM_001330752.2:c.1282G>T
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NP_001317681.1:p.Ala428Ser
|
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NM_001354825.2:c.1333G>T
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NP_001341754.1:p.Ala445Ser
|
|
NM_001354826.2:c.937G>T
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NP_001341755.1:p.Ala313Ser
|
|
NM_001354827.2:c.1333G>T
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NP_001341756.1:p.Ala445Ser
|
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NR_148981.2:n.1921G>T
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NR_148982.2:n.1994G>T
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NR_148983.2:n.2147G>T
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NR_148984.2:n.1439G>T
|
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NR_148985.2:n.2059G>T
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NR_148986.2:n.2064G>T
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|
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NR_148987.2:n.2146G>T
|
|
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NM_001330753.2:c.937G>T
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NP_001317682.1:p.Ala313Ser
|
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