ENST00000355943.8:c.1011T>C
MANE Select
|
ENSP00000348211.3:p.Val337=
|
|
ENST00000355943.7:c.1011T>C
|
ENSP00000348211.3:p.Val337=
|
|
ENST00000447245.6:c.768T>C
|
ENSP00000399717.2:p.Val256=
|
|
ENST00000502462.6:n.1327T>C
|
|
|
ENST00000504098.1:c.573T>C
|
ENSP00000425708.1:p.Val191=
|
|
ENST00000509432.1:c.372T>C
|
ENSP00000426604.1:p.Val124=
|
|
ENST00000513706.2:n.2611T>C
|
|
|
ENST00000513807.5:c.525T>C
|
ENSP00000421134.1:p.Val175=
|
|
NM_001303249.1:c.768T>C
|
NP_001290178.1:p.Val256=
|
|
NM_001303250.1:c.738T>C
|
NP_001290179.1:p.Val246=
|
|
NM_138773.2:c.1011T>C
|
NP_620128.1:p.Val337=
|
|
NM_001303249.2:c.768T>C
|
NP_001290178.1:p.Val256=
|
|
NM_001303250.2:c.738T>C
|
NP_001290179.1:p.Val246=
|
|
NM_138773.3:c.1011T>C
|
NP_620128.1:p.Val337=
|
|
NR_138151.1:n.1285T>C
|
|
|
NM_138773.4:c.1011T>C
MANE Select
|
NP_620128.1:p.Val337=
|
|
NM_001303249.3:c.768T>C
|
NP_001290178.1:p.Val256=
|
|
NM_001303250.3:c.738T>C
|
NP_001290179.1:p.Val246=
|
|
NR_138151.2:n.1250T>C
|
|
|