ENST00000261937.11:c.3901G>C
MANE Select
|
ENSP00000261937.6:p.Gly1301Arg
|
|
ENST00000261937.10:c.3901G>C
|
ENSP00000261937.6:p.Gly1301Arg
|
|
ENST00000502603.5:n.601G>C
|
|
|
NM_182925.4:c.3901G>C
|
NP_891555.2:p.Gly1301Arg
|
|
XM_011534477.1:c.4150G>C
|
XP_011532779.1:p.Gly1384Arg
|
|
XM_011534478.1:c.4132G>C
|
XP_011532780.1:p.Gly1378Arg
|
|
XM_011534479.1:c.*47G>C
|
XP_011532781.1:n.*47G>C
|
|
XM_011534482.1:c.3919G>C
|
XP_011532784.1:p.Gly1307Arg
|
|
XM_011534483.1:c.3841G>C
|
XP_011532785.1:p.Gly1281Arg
|
|
XM_011534484.1:c.3442G>C
|
XP_011532786.1:p.Gly1148Arg
|
|
XR_941095.1:n.4187G>C
|
|
|
XM_011534478.3:c.4132G>C
|
XP_011532780.1:p.Gly1378Arg
|
|
XM_011534484.2:c.3442G>C
|
XP_011532786.1:p.Gly1148Arg
|
|
XM_017009263.1:c.*47G>C
|
XP_016864752.1:n.*47G>C
|
|
XM_017009268.1:c.3823G>C
|
XP_016864757.1:p.Gly1275Arg
|
|
XR_001742050.2:n.4391G>C
|
|
|
NM_182925.5:c.3901G>C
MANE Select
|
NP_891555.2:p.Gly1301Arg
|
|