ENST00000265104.5:c.9274G>C
MANE Select
|
ENSP00000265104.4:p.Gly3092Arg
|
|
ENST00000681290.1:c.9229G>C
|
ENSP00000505288.1:p.Gly3077Arg
|
|
ENST00000265104.4:c.9274G>C
|
ENSP00000265104.4:p.Gly3092Arg
|
|
NM_001369.2:c.9274G>C
|
NP_001360.1:p.Gly3092Arg
|
|
XM_005248262.2:c.9229G>C
|
XP_005248319.1:p.Gly3077Arg
|
|
XM_005248262.3:c.9382G>C
|
XP_005248319.2:p.Gly3128Arg
|
|
XM_017009177.1:c.9382G>C
|
XP_016864666.1:p.Gly3128Arg
|
|
XM_017009178.1:c.8287G>C
|
XP_016864667.1:p.Gly2763Arg
|
|
XM_017009179.2:c.8287G>C
|
XP_016864668.1:p.Gly2763Arg
|
|
XM_017009180.1:c.9382G>C
|
XP_016864669.1:p.Gly3128Arg
|
|
XM_017009181.1:c.9382G>C
|
XP_016864670.1:p.Gly3128Arg
|
|
XM_017009182.1:c.9382G>C
|
XP_016864671.1:p.Gly3128Arg
|
|
XM_017009183.1:c.9382G>C
|
XP_016864672.1:p.Gly3128Arg
|
|
XM_017009185.1:c.4471G>C
|
XP_016864674.1:p.Gly1491Arg
|
|
XM_017009186.1:c.4024G>C
|
XP_016864675.1:p.Gly1342Arg
|
|
XM_017009188.1:c.3361G>C
|
XP_016864677.1:p.Gly1121Arg
|
|
XM_024454388.1:c.8287G>C
|
XP_024310156.1:p.Gly2763Arg
|
|
XM_024454389.1:c.7876G>C
|
XP_024310157.1:p.Gly2626Arg
|
|
NM_001369.3:c.9274G>C
MANE Select
|
NP_001360.1:p.Gly3092Arg
|
|