ENST00000394975.3:c.*96G>A
MANE Select
|
ENSP00000378426.2:n.*96G>A
|
|
ENST00000300851.10:c.*199G>A
|
ENSP00000300851.6:n.*199G>A
|
|
ENST00000319788.11:c.*199G>A
|
ENSP00000326135.7:n.*199G>A
|
|
ENST00000354895.4:c.*199G>A
|
ENSP00000346969.4:n.*199G>A
|
|
ENST00000394975.2:c.*96G>A
|
ENSP00000378426.2:n.*96G>A
|
|
ENST00000420057.2:c.550G>A
|
|
|
ENST00000529564.1:c.283+2274G>A
|
ENSP00000431371.1:n.283+2274G>A
|
|
ENST00000532364.1:c.173+3519G>A
|
ENSP00000460316.1:n.173+3519G>A
|
|
ENST00000533518.5:c.407+54G>A
|
|
|
NM_001311311.1:c.*96G>A
|
NP_001298240.1:n.*96G>A
|
|
NM_024006.4:c.*96G>A
|
NP_076869.1:n.*96G>A
|
|
NM_024006.5:c.*96G>A
|
NP_076869.1:n.*96G>A
|
|
NM_206824.1:c.*199G>A
|
NP_996560.1:n.*199G>A
|
|
NM_206824.2:c.*199G>A
|
NP_996560.1:n.*199G>A
|
|
XM_011545944.1:c.*96G>A
|
XP_011544246.1:n.*96G>A
|
|
XM_011545945.1:c.*199G>A
|
XP_011544247.1:n.*199G>A
|
|
XR_950848.1:n.1376G>A
|
|
|
NM_024006.6:c.*96G>A
MANE Select
|
NP_076869.1:n.*96G>A
|
|
NM_001311311.2:c.*96G>A
|
NP_001298240.1:n.*96G>A
|
|
NM_206824.3:c.*199G>A
|
NP_996560.1:n.*199G>A
|
|