ENST00000261937.11:c.4014G>C
MANE Select
|
ENSP00000261937.6:p.Gly1338=
|
|
ENST00000261937.10:c.4014G>C
|
ENSP00000261937.6:p.Gly1338=
|
|
ENST00000502603.5:n.714G>C
|
|
|
NM_182925.4:c.4014G>C
|
NP_891555.2:p.Gly1338=
|
|
XM_011534477.1:c.4263G>C
|
XP_011532779.1:p.Gly1421=
|
|
XM_011534478.1:c.4245G>C
|
XP_011532780.1:p.Gly1415=
|
|
XM_011534482.1:c.4032G>C
|
XP_011532784.1:p.Gly1344=
|
|
XM_011534483.1:c.3954G>C
|
XP_011532785.1:p.Gly1318=
|
|
XM_011534484.1:c.3555G>C
|
XP_011532786.1:p.Gly1185=
|
|
XR_941095.1:n.4300G>C
|
|
|
XM_011534478.3:c.4245G>C
|
XP_011532780.1:p.Gly1415=
|
|
XM_011534484.2:c.3555G>C
|
XP_011532786.1:p.Gly1185=
|
|
XM_017009263.1:c.*160G>C
|
XP_016864752.1:n.*160G>C
|
|
XM_017009268.1:c.3936G>C
|
XP_016864757.1:p.Gly1312=
|
|
XR_001742050.2:n.4504G>C
|
|
|
NM_182925.5:c.4014G>C
MANE Select
|
NP_891555.2:p.Gly1338=
|
|