ENST00000474381.2:n.2760C>T
|
|
|
ENST00000481849.6:n.2186C>T
|
|
|
ENST00000497377.6:n.2186C>T
|
|
|
ENST00000640094.2:c.713C>T
|
ENSP00000491275.2:p.Thr238Ile
|
|
ENST00000696558.1:c.782C>T
|
ENSP00000512716.1:n.782C>T
|
|
ENST00000696559.1:c.713C>T
|
ENSP00000512717.1:p.Thr238Ile
|
|
ENST00000696560.1:c.713C>T
|
ENSP00000512718.1:p.Thr238Ile
|
|
ENST00000696561.1:c.713C>T
|
ENSP00000512719.1:p.Thr238Ile
|
|
ENST00000696562.1:c.713C>T
|
ENSP00000512720.1:p.Thr238Ile
|
|
ENST00000412585.7:c.713C>T
MANE Select
|
ENSP00000399168.2:p.Thr238Ile
|
|
ENST00000412585.6:c.713C>T
|
ENSP00000399168.2:p.Thr238Ile
|
|
ENST00000463574.1:n.304C>T
|
|
|
ENST00000498007.1:n.979C>T
|
|
|
NM_005514.6:c.713C>T
|
NP_005505.2:p.Thr238Ile
|
|
XM_011514556.1:c.746C>T
|
XP_011512858.1:p.Thr249Ile
|
|
XM_011514557.1:c.713C>T
|
XP_011512859.1:p.Thr238Ile
|
|
XR_926175.1:n.1152C>T
|
|
|
NM_005514.7:c.713C>T
|
NP_005505.2:p.Thr238Ile
|
|
NM_005514.8:c.713C>T
MANE Select
|
NP_005505.2:p.Thr238Ile
|
|