ENST00000348931.9:c.444A>G
MANE Select
|
ENSP00000335384.5:p.Val148=
|
|
ENST00000348931.8:c.444A>G
|
ENSP00000335384.5:p.Val148=
|
|
ENST00000377940.3:c.378A>G
|
ENSP00000367174.3:p.Val126=
|
|
ENST00000583811.5:c.90A>G
|
ENSP00000462463.1:p.Val30=
|
|
ENST00000584588.5:c.406+682A>G
|
ENSP00000462067.1:n.406+682A>G
|
|
NM_198844.2:c.378A>G
|
NP_942141.2:p.Val126=
|
|
NM_199321.2:c.444A>G
|
NP_955353.1:p.Val148=
|
|
XM_011524298.1:c.444A>G
|
XP_011522600.1:p.Val148=
|
|
XR_002957959.1:n.635A>G
|
|
|
NM_198844.3:c.378A>G
|
NP_942141.2:p.Val126=
|
|
NM_199321.3:c.444A>G
MANE Select
|
NP_955353.1:p.Val148=
|
|