ENST00000394975.3:c.472G>C
MANE Select
|
ENSP00000378426.2:p.Gly158Arg
|
|
ENST00000300851.10:c.*83G>C
|
ENSP00000300851.6:n.*83G>C
|
|
ENST00000319788.11:c.*83G>C
|
ENSP00000326135.7:n.*83G>C
|
|
ENST00000354895.4:c.*83G>C
|
ENSP00000346969.4:n.*83G>C
|
|
ENST00000394971.7:c.*83G>C
|
ENSP00000378422.3:n.*83G>C
|
|
ENST00000394975.2:c.472G>C
|
ENSP00000378426.2:p.Gly158Arg
|
|
ENST00000420057.2:c.434G>C
|
|
|
ENST00000529564.1:c.283+2158G>C
|
ENSP00000431371.1:n.283+2158G>C
|
|
ENST00000532364.1:c.173+3403G>C
|
ENSP00000460316.1:n.173+3403G>C
|
|
ENST00000533518.5:c.345G>C
|
|
|
NM_001311311.1:c.556G>C
|
NP_001298240.1:p.Gly186Arg
|
|
NM_024006.4:c.472G>C
|
NP_076869.1:p.Gly158Arg
|
|
NM_024006.5:c.472G>C
|
NP_076869.1:p.Gly158Arg
|
|
NM_206824.1:c.*83G>C
|
NP_996560.1:n.*83G>C
|
|
NM_206824.2:c.*83G>C
|
NP_996560.1:n.*83G>C
|
|
XM_011545944.1:c.472G>C
|
XP_011544246.1:p.Gly158Arg
|
|
XM_011545945.1:c.*83G>C
|
XP_011544247.1:n.*83G>C
|
|
XR_950848.1:n.1260G>C
|
|
|
NM_024006.6:c.472G>C
MANE Select
|
NP_076869.1:p.Gly158Arg
|
|
NM_001311311.2:c.556G>C
|
NP_001298240.1:p.Gly186Arg
|
|
NM_206824.3:c.*83G>C
|
NP_996560.1:n.*83G>C
|
|