ENST00000474381.2:n.2988G>T
|
|
|
ENST00000481849.6:n.2507G>T
|
|
|
ENST00000497377.6:n.2414G>T
|
|
|
ENST00000640094.2:c.895+139G>T
|
ENSP00000491275.2:n.895+139G>T
|
|
ENST00000696558.1:c.1010G>T
|
ENSP00000512716.1:n.1010G>T
|
|
ENST00000696559.1:c.941G>T
|
ENSP00000512717.1:p.Gly314Val
|
|
ENST00000696560.1:c.941G>T
|
ENSP00000512718.1:p.Gly314Val
|
|
ENST00000696561.1:c.941G>T
|
ENSP00000512719.1:p.Gly314Val
|
|
ENST00000696562.1:c.941G>T
|
ENSP00000512720.1:p.Gly314Val
|
|
ENST00000412585.7:c.941G>T
MANE Select
|
ENSP00000399168.2:p.Gly314Val
|
|
ENST00000640094.1:c.88+139G>T
|
ENSP00000491275.1:n.88+139G>T
|
|
ENST00000412585.6:c.941G>T
|
ENSP00000399168.2:p.Gly314Val
|
|
ENST00000463574.1:n.532G>T
|
|
|
NM_005514.6:c.941G>T
|
NP_005505.2:p.Gly314Val
|
|
XM_011514556.1:c.974G>T
|
XP_011512858.1:p.Gly325Val
|
|
XM_011514557.1:c.895+139G>T
|
XP_011512859.1:n.895+139G>T
|
|
XR_926175.1:n.1380G>T
|
|
|
NM_005514.7:c.941G>T
|
NP_005505.2:p.Gly314Val
|
|
NM_005514.8:c.941G>T
MANE Select
|
NP_005505.2:p.Gly314Val
|
|