ENST00000315757.9:c.1356C>G
MANE Select
|
ENSP00000327290.7:p.Gly452=
|
|
ENST00000315757.8:c.1356C>G
|
ENSP00000327290.7:p.Gly452=
|
|
ENST00000423218.6:c.1356C>G
|
ENSP00000403392.2:p.Gly452=
|
|
ENST00000566429.1:n.245C>G
|
|
|
ENST00000569346.5:n.335C>G
|
|
|
NM_001004439.1:c.1356C>G
|
NP_001004439.1:p.Gly452=
|
|
XM_005254228.2:c.1050C>G
|
XP_005254285.1:p.Gly350=
|
|
XM_011521363.1:c.1149C>G
|
XP_011519665.1:p.Gly383=
|
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XM_005254228.3:c.1050C>G
|
XP_005254285.1:p.Gly350=
|
|
XM_011521363.2:c.1149C>G
|
XP_011519665.1:p.Gly383=
|
|
NM_001004439.2:c.1356C>G
MANE Select
|
NP_001004439.1:p.Gly452=
|
|