ENST00000474370.2:n.2394A>G
|
|
|
ENST00000492391.2:n.1545A>G
|
|
|
ENST00000682645.1:n.3492A>G
|
|
|
ENST00000683432.1:c.*596A>G
|
ENSP00000508174.1:n.*596A>G
|
|
ENST00000684207.1:c.421A>G
|
ENSP00000506942.1:p.Met141Val
|
|
ENST00000297157.8:c.421A>G
MANE Select
|
ENSP00000297157.3:p.Met141Val
|
|
ENST00000297157.7:c.421A>G
|
ENSP00000297157.3:p.Met141Val
|
|
ENST00000448915.1:c.319A>G
|
ENSP00000411577.1:p.Met107Val
|
|
NM_203288.1:c.421A>G
|
NP_976033.1:p.Met141Val
|
|
XM_011515468.1:c.319A>G
|
XP_011513770.1:p.Met107Val
|
|
XM_011515468.3:c.319A>G
|
XP_011513770.1:p.Met107Val
|
|
NM_203288.2:c.421A>G
MANE Select
|
NP_976033.1:p.Met141Val
|
|