ENST00000565588.6:c.353G>C
|
ENSP00000455537.2:p.Ser118Thr
|
|
ENST00000696156.1:c.269G>C
|
ENSP00000512446.1:p.Ser90Thr
|
|
ENST00000696157.1:c.353G>C
|
ENSP00000512447.1:p.Ser118Thr
|
|
ENST00000696158.1:c.353G>C
|
ENSP00000512448.1:p.Ser118Thr
|
|
ENST00000696159.1:c.353G>C
|
ENSP00000512449.1:p.Ser118Thr
|
|
ENST00000696160.1:c.353G>C
|
ENSP00000512450.1:p.Ser118Thr
|
|
ENST00000696161.1:c.483G>C
|
ENSP00000512451.1:p.Glu161Asp
|
|
ENST00000696162.1:c.353G>C
|
ENSP00000512452.1:p.Ser118Thr
|
|
ENST00000696163.1:c.302G>C
|
ENSP00000512453.1:p.Ser101Thr
|
|
ENST00000261623.8:c.353G>C
MANE Select
|
ENSP00000261623.3:p.Ser118Thr
|
|
ENST00000261623.7:c.353G>C
|
ENSP00000261623.3:p.Ser118Thr
|
|
ENST00000563526.5:n.885G>C
|
|
|
ENST00000565588.5:c.137G>C
|
|
|
ENST00000566229.1:c.342G>C
|
ENSP00000457060.1:p.Glu114Asp
|
|
ENST00000566534.5:n.932G>C
|
|
|
ENST00000567174.5:c.353G>C
|
ENSP00000454951.1:p.Ser118Thr
|
|
ENST00000568278.1:c.437G>C
|
|
|
ENST00000569359.5:c.353G>C
|
ENSP00000456079.1:p.Ser118Thr
|
|
NM_000101.3:c.353G>C
|
NP_000092.2:p.Ser118Thr
|
|
XM_011522905.1:c.353G>C
|
XP_011521207.1:p.Ser118Thr
|
|
XM_011522905.3:c.353G>C
|
XP_011521207.1:p.Ser118Thr
|
|
NM_000101.4:c.353G>C
MANE Select
|
NP_000092.2:p.Ser118Thr
|
|