ENST00000304895.9:c.1855G>T
MANE Select
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ENSP00000302728.4:p.Ala619Ser
|
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ENST00000304895.8:c.1855G>T
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ENSP00000302728.4:p.Ala619Ser
|
|
ENST00000421103.5:c.1417G>T
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ENSP00000391390.1:p.Ala473Ser
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ENST00000430730.5:c.*1122G>T
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ENSP00000411859.1:n.*1122G>T
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ENST00000447929.5:c.*1235G>T
|
ENSP00000411262.1:n.*1235G>T
|
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ENST00000466883.5:n.2245G>T
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|
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NM_000181.3:c.1855G>T
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NP_000172.2:p.Ala619Ser
|
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NM_001284290.1:c.1417G>T
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NP_001271219.1:p.Ala473Ser
|
|
NM_001293104.1:c.1285G>T
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NP_001280033.1:p.Ala429Ser
|
|
NM_001293105.1:c.1198G>T
|
NP_001280034.1:p.Ala400Ser
|
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NR_120531.1:n.1901G>T
|
|
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XM_005250297.3:c.1702G>T
|
XP_005250354.1:p.Ala568Ser
|
|
XM_011516113.1:c.1354G>T
|
XP_011514415.1:p.Ala452Ser
|
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XM_011516114.1:c.1183G>T
|
XP_011514416.1:p.Ala395Ser
|
|
XM_005250297.4:c.1702G>T
|
XP_005250354.1:p.Ala568Ser
|
|
XM_011516114.2:c.1183G>T
|
XP_011514416.1:p.Ala395Ser
|
|
XM_017012091.1:c.1201G>T
|
XP_016867580.1:p.Ala401Ser
|
|
XM_017012092.1:c.1132G>T
|
XP_016867581.1:p.Ala378Ser
|
|
XM_017012093.2:c.1030G>T
|
XP_016867582.1:p.Ala344Ser
|
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XR_001744658.2:n.1662G>T
|
|
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XR_001744659.2:n.1775G>T
|
|
|
XR_001744660.2:n.1707G>T
|
|
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XR_001744661.2:n.1622G>T
|
|
|
XR_927461.3:n.1860G>T
|
|
|
NM_000181.4:c.1855G>T
MANE Select
|
NP_000172.2:p.Ala619Ser
|
|
NM_001284290.2:c.1417G>T
|
NP_001271219.1:p.Ala473Ser
|
|
NM_001293104.2:c.1285G>T
|
NP_001280033.1:p.Ala429Ser
|
|
NM_001293105.2:c.1198G>T
|
NP_001280034.1:p.Ala400Ser
|
|
NR_120531.2:n.1800G>T
|
|
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