ENST00000348931.9:c.447T>C
MANE Select
|
ENSP00000335384.5:p.Arg149=
|
|
ENST00000348931.8:c.447T>C
|
ENSP00000335384.5:p.Arg149=
|
|
ENST00000377940.3:c.381T>C
|
ENSP00000367174.3:p.Arg127=
|
|
ENST00000583811.5:c.93T>C
|
ENSP00000462463.1:p.Arg31=
|
|
ENST00000584588.5:c.406+685T>C
|
ENSP00000462067.1:n.406+685T>C
|
|
NM_198844.2:c.381T>C
|
NP_942141.2:p.Arg127=
|
|
NM_199321.2:c.447T>C
|
NP_955353.1:p.Arg149=
|
|
XM_011524298.1:c.447T>C
|
XP_011522600.1:p.Arg149=
|
|
XR_002957959.1:n.638T>C
|
|
|
NM_198844.3:c.381T>C
|
NP_942141.2:p.Arg127=
|
|
NM_199321.3:c.447T>C
MANE Select
|
NP_955353.1:p.Arg149=
|
|