ENST00000306010.8:c.367+3374G>T
|
ENSP00000302111.7:n.367+3374G>T
|
|
ENST00000651593.1:c.274+3374G>T
MANE Select
|
ENSP00000498729.1:n.274+3374G>T
|
|
ENST00000306010.7:c.367+3374G>T
|
ENSP00000302111.7:n.367+3374G>T
|
|
ENST00000462672.1:n.435+3374G>T
|
|
|
NM_002412.3:c.367+3374G>T
|
NP_002403.2:n.367+3374G>T
|
|
NM_002412.4:c.367+3374G>T
|
NP_002403.2:n.367+3374G>T
|
|
XM_005252682.2:c.274+3374G>T
|
XP_005252739.1:n.274+3374G>T
|
|
XM_006717863.2:c.97+3374G>T
|
XP_006717926.1:n.97+3374G>T
|
|
XM_011539817.1:c.283+3374G>T
|
XP_011538119.1:n.283+3374G>T
|
|
NM_002412.5:c.274+3374G>T
MANE Select
|
NP_002403.3:n.274+3374G>T
|
|
XM_017016275.1:c.97+3374G>T
|
XP_016871764.1:n.97+3374G>T
|
|
XR_946467.2:n.3368G>T
|
|
|