ENST00000315757.9:c.1330G>T
MANE Select
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ENSP00000327290.7:p.Gly444Ter
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ENST00000315757.8:c.1330G>T
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ENSP00000327290.7:p.Gly444Ter
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|
ENST00000423218.6:c.1330G>T
|
ENSP00000403392.2:p.Gly444Ter
|
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ENST00000566429.1:n.219G>T
|
|
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ENST00000569346.5:n.309G>T
|
|
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NM_001004439.1:c.1330G>T
|
NP_001004439.1:p.Gly444Ter
|
|
XM_005254228.2:c.1024G>T
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XP_005254285.1:p.Gly342Ter
|
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XM_011521363.1:c.1123G>T
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XP_011519665.1:p.Gly375Ter
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XM_005254228.3:c.1024G>T
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XP_005254285.1:p.Gly342Ter
|
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XM_011521363.2:c.1123G>T
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XP_011519665.1:p.Gly375Ter
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|
NM_001004439.2:c.1330G>T
MANE Select
|
NP_001004439.1:p.Gly444Ter
|
|