ENST00000261937.11:c.4012G>C
MANE Select
|
ENSP00000261937.6:p.Gly1338Arg
|
|
ENST00000261937.10:c.4012G>C
|
ENSP00000261937.6:p.Gly1338Arg
|
|
ENST00000502603.5:n.712G>C
|
|
|
NM_182925.4:c.4012G>C
|
NP_891555.2:p.Gly1338Arg
|
|
XM_011534477.1:c.4261G>C
|
XP_011532779.1:p.Gly1421Arg
|
|
XM_011534478.1:c.4243G>C
|
XP_011532780.1:p.Gly1415Arg
|
|
XM_011534482.1:c.4030G>C
|
XP_011532784.1:p.Gly1344Arg
|
|
XM_011534483.1:c.3952G>C
|
XP_011532785.1:p.Gly1318Arg
|
|
XM_011534484.1:c.3553G>C
|
XP_011532786.1:p.Gly1185Arg
|
|
XR_941095.1:n.4298G>C
|
|
|
XM_011534478.3:c.4243G>C
|
XP_011532780.1:p.Gly1415Arg
|
|
XM_011534484.2:c.3553G>C
|
XP_011532786.1:p.Gly1185Arg
|
|
XM_017009263.1:c.*158G>C
|
XP_016864752.1:n.*158G>C
|
|
XM_017009268.1:c.3934G>C
|
XP_016864757.1:p.Gly1312Arg
|
|
XR_001742050.2:n.4502G>C
|
|
|
NM_182925.5:c.4012G>C
MANE Select
|
NP_891555.2:p.Gly1338Arg
|
|