ENST00000370938.8:c.1217A>C
MANE Select
|
ENSP00000359976.3:p.Ter406Ser
|
|
ENST00000346806.2:c.1085A>C
|
ENSP00000311554.2:p.Ter362Ser
|
|
ENST00000370938.7:c.1217A>C
|
ENSP00000359976.3:p.Ter406Ser
|
|
ENST00000411986.6:c.1121A>C
|
ENSP00000413407.2:p.Ter374Ser
|
|
ENST00000482383.1:n.492A>C
|
|
|
NM_001190463.1:c.1121A>C
|
NP_001177392.1:p.Ter374Ser
|
|
NM_001902.5:c.1217A>C
|
NP_001893.2:p.Ter406Ser
|
|
NM_153742.4:c.1085A>C
|
NP_714964.2:p.Ter362Ser
|
|
XM_005270509.2:c.890A>C
|
XP_005270566.1:p.Ter297Ser
|
|
XM_011540787.1:c.647A>C
|
XP_011539089.1:p.Ter216Ser
|
|
XM_005270509.3:c.890A>C
|
XP_005270566.1:p.Ter297Ser
|
|
XM_017000416.2:c.647A>C
|
XP_016855905.1:p.Ter216Ser
|
|
NM_001902.6:c.1217A>C
MANE Select
|
NP_001893.2:p.Ter406Ser
|
|
NM_001190463.2:c.1121A>C
|
NP_001177392.1:p.Ter374Ser
|
|
NM_153742.5:c.1085A>C
|
NP_714964.2:p.Ter362Ser
|
|