ENST00000264867.7:c.1207G>T
MANE Select
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ENSP00000264867.2:p.Glu403Ter
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ENST00000264867.6:c.1207G>T
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ENSP00000264867.2:p.Glu403Ter
|
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ENST00000506055.5:c.*422G>T
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ENSP00000423075.1:n.*422G>T
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ENST00000509702.5:n.1247G>T
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|
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ENST00000613098.4:c.826G>T
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ENSP00000481498.1:p.Glu276Ter
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NM_013261.3:c.1207G>T
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NP_037393.1:p.Glu403Ter
|
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XM_005248130.2:c.1222G>T
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XP_005248187.1:p.Glu408Ter
|
|
XM_005248131.3:c.1219G>T
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XP_005248188.1:p.Glu407Ter
|
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XM_005248132.1:c.1198G>T
|
XP_005248189.1:p.Glu400Ter
|
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XM_005248134.3:c.1222G>T
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XP_005248191.1:p.Glu408Ter
|
|
XM_011513764.1:c.1207G>T
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XP_011512066.1:p.Glu403Ter
|
|
XM_011513765.1:c.1171G>T
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XP_011512067.1:p.Glu391Ter
|
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XM_011513766.1:c.1102G>T
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XP_011512068.1:p.Glu368Ter
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|
XM_011513767.1:c.1102G>T
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XP_011512069.1:p.Glu368Ter
|
|
XM_011513768.1:c.1102G>T
|
XP_011512070.1:p.Glu368Ter
|
|
XM_011513769.1:c.1222G>T
|
XP_011512071.1:p.Glu408Ter
|
|
XM_011513770.1:c.826G>T
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XP_011512072.1:p.Glu276Ter
|
|
XM_011513771.1:c.826G>T
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XP_011512073.1:p.Glu276Ter
|
|
NM_001330751.1:c.1222G>T
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NP_001317680.1:p.Glu408Ter
|
|
NM_001330752.1:c.1171G>T
|
NP_001317681.1:p.Glu391Ter
|
|
NM_001330753.1:c.826G>T
|
NP_001317682.1:p.Glu276Ter
|
|
NM_001354825.1:c.1222G>T
|
NP_001341754.1:p.Glu408Ter
|
|
NM_001354826.1:c.826G>T
|
NP_001341755.1:p.Glu276Ter
|
|
NM_001354827.1:c.1222G>T
|
NP_001341756.1:p.Glu408Ter
|
|
NM_013261.4:c.1207G>T
|
NP_037393.1:p.Glu403Ter
|
|
NR_148981.1:n.1734G>T
|
|
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NR_148982.1:n.1807G>T
|
|
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NR_148983.1:n.1960G>T
|
|
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NR_148984.1:n.1358G>T
|
|
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NR_148985.1:n.1872G>T
|
|
|
NR_148986.1:n.1877G>T
|
|
|
NR_148987.1:n.1959G>T
|
|
|
XM_005248131.5:c.1219G>T
|
XP_005248188.1:p.Glu407Ter
|
|
XM_005248134.4:c.1222G>T
|
XP_005248191.1:p.Glu408Ter
|
|
XM_011513769.2:c.1222G>T
|
XP_011512071.1:p.Glu408Ter
|
|
XM_024453878.1:c.1222G>T
|
XP_024309646.1:p.Glu408Ter
|
|
NM_013261.5:c.1207G>T
MANE Select
|
NP_037393.1:p.Glu403Ter
|
|
NM_001330751.2:c.1222G>T
|
NP_001317680.1:p.Glu408Ter
|
|
NM_001330752.2:c.1171G>T
|
NP_001317681.1:p.Glu391Ter
|
|
NM_001354825.2:c.1222G>T
|
NP_001341754.1:p.Glu408Ter
|
|
NM_001354826.2:c.826G>T
|
NP_001341755.1:p.Glu276Ter
|
|
NM_001354827.2:c.1222G>T
|
NP_001341756.1:p.Glu408Ter
|
|
NR_148981.2:n.1810G>T
|
|
|
NR_148982.2:n.1883G>T
|
|
|
NR_148983.2:n.2036G>T
|
|
|
NR_148984.2:n.1328G>T
|
|
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NR_148985.2:n.1948G>T
|
|
|
NR_148986.2:n.1953G>T
|
|
|
NR_148987.2:n.2035G>T
|
|
|
NM_001330753.2:c.826G>T
|
NP_001317682.1:p.Glu276Ter
|
|