ENST00000474381.2:n.3336G>A
|
|
|
ENST00000481849.6:n.3296G>A
|
|
|
ENST00000497377.6:n.3203G>A
|
|
|
ENST00000696558.1:c.1358G>A
|
ENSP00000512716.1:n.1358G>A
|
|
ENST00000696559.1:c.*200G>A
|
ENSP00000512717.1:n.*200G>A
|
|
ENST00000696560.1:c.*200G>A
|
ENSP00000512718.1:n.*200G>A
|
|
ENST00000696561.1:c.*200G>A
|
ENSP00000512719.1:n.*200G>A
|
|
ENST00000696562.1:c.*200G>A
|
ENSP00000512720.1:n.*200G>A
|
|
ENST00000412585.7:c.*200G>A
MANE Select
|
ENSP00000399168.2:n.*200G>A
|
|
ENST00000412585.6:c.*200G>A
|
ENSP00000399168.2:n.*200G>A
|
|
ENST00000481849.5:n.524G>A
|
|
|
ENST00000497377.5:n.688G>A
|
|
|
NM_005514.6:c.*200G>A
|
NP_005505.2:n.*200G>A
|
|
XM_011514556.1:c.*200G>A
|
XP_011512858.1:n.*200G>A
|
|
XM_011514557.1:c.*200G>A
|
XP_011512859.1:n.*200G>A
|
|
XR_926175.1:n.1728G>A
|
|
|
NM_005514.7:c.*200G>A
|
NP_005505.2:n.*200G>A
|
|
NM_005514.8:c.*200G>A
MANE Select
|
NP_005505.2:n.*200G>A
|
|