ENST00000315757.9:c.1314G>A
MANE Select
|
ENSP00000327290.7:p.Gly438=
|
|
ENST00000315757.8:c.1314G>A
|
ENSP00000327290.7:p.Gly438=
|
|
ENST00000423218.6:c.1314G>A
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ENSP00000403392.2:p.Gly438=
|
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ENST00000566429.1:n.203G>A
|
|
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ENST00000569346.5:n.293G>A
|
|
|
NM_001004439.1:c.1314G>A
|
NP_001004439.1:p.Gly438=
|
|
XM_005254228.2:c.1008G>A
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XP_005254285.1:p.Gly336=
|
|
XM_011521363.1:c.1107G>A
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XP_011519665.1:p.Gly369=
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XM_005254228.3:c.1008G>A
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XP_005254285.1:p.Gly336=
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|
XM_011521363.2:c.1107G>A
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XP_011519665.1:p.Gly369=
|
|
NM_001004439.2:c.1314G>A
MANE Select
|
NP_001004439.1:p.Gly438=
|
|