ENST00000673739.2:c.*2892G>C
|
ENSP00000501110.2:n.*2892G>C
|
|
ENST00000673882.2:c.*2681G>C
|
ENSP00000501253.2:n.*2681G>C
|
|
ENST00000673739.1:c.3300G>C
|
ENSP00000501110.1:n.3300G>C
|
|
ENST00000673882.1:c.3089G>C
|
ENSP00000501253.1:n.3089G>C
|
|
ENST00000233242.5:c.3586G>C
MANE Select
|
ENSP00000233242.1:p.Asp1196His
|
|
ENST00000616098.4:c.3586G>C
|
ENSP00000477990.1:p.Asp1196His
|
|
NM_000384.2:c.3586G>C
|
NP_000375.2:p.Asp1196His
|
|
XM_011532809.1:c.3586G>C
|
XP_011531111.1:p.Asp1196His
|
|
NM_000384.3:c.3586G>C
MANE Select
|
NP_000375.3:p.Asp1196His
|
|