ENST00000474381.2:n.3098G>C
|
|
|
ENST00000481849.6:n.3058G>C
|
|
|
ENST00000497377.6:n.2965G>C
|
|
|
ENST00000640094.2:c.934G>C
|
ENSP00000491275.2:p.Asp312His
|
|
ENST00000696558.1:c.1120G>C
|
ENSP00000512716.1:n.1120G>C
|
|
ENST00000696559.1:c.1051G>C
|
ENSP00000512717.1:p.Asp351His
|
|
ENST00000696560.1:c.1051G>C
|
ENSP00000512718.1:p.Asp351His
|
|
ENST00000696561.1:c.1051G>C
|
ENSP00000512719.1:p.Asp351His
|
|
ENST00000696562.1:c.1051G>C
|
ENSP00000512720.1:p.Asp351His
|
|
ENST00000412585.7:c.1051G>C
MANE Select
|
ENSP00000399168.2:p.Asp351His
|
|
ENST00000640094.1:c.127G>C
|
ENSP00000491275.1:p.Asp43His
|
|
ENST00000412585.6:c.1051G>C
|
ENSP00000399168.2:p.Asp351His
|
|
ENST00000481849.5:n.286G>C
|
|
|
ENST00000497377.5:n.450G>C
|
|
|
NM_005514.6:c.1051G>C
|
NP_005505.2:p.Asp351His
|
|
XM_011514556.1:c.1084G>C
|
XP_011512858.1:p.Asp362His
|
|
XM_011514557.1:c.934G>C
|
XP_011512859.1:p.Asp312His
|
|
XR_926175.1:n.1490G>C
|
|
|
NM_005514.7:c.1051G>C
|
NP_005505.2:p.Asp351His
|
|
NM_005514.8:c.1051G>C
MANE Select
|
NP_005505.2:p.Asp351His
|
|