ENST00000369538.4:c.1187G>C
|
ENSP00000358551.4:p.Gly396Ala
|
|
ENST00000520113.7:c.1199G>C
MANE Select
|
ENSP00000430075.3:p.Gly400Ala
|
|
ENST00000637080.1:c.982G>C
|
ENSP00000489753.1:n.982G>C
|
|
ENST00000639077.1:n.864G>C
|
|
|
ENST00000369538.3:c.1286G>C
|
ENSP00000358551.3:p.Gly429Ala
|
|
ENST00000520113.6:c.1298G>C
|
ENSP00000430075.2:p.Gly433Ala
|
|
NM_000036.2:c.1298G>C
|
NP_000027.2:p.Gly433Ala
|
|
NM_001172626.1:c.1286G>C
|
NP_001166097.1:p.Gly429Ala
|
|
NM_000036.3:c.1199G>C
MANE Select
|
NP_000027.3:p.Gly400Ala
|
|
NM_001172626.2:c.1187G>C
|
NP_001166097.2:p.Gly396Ala
|
|