ENST00000281928.9:c.3015G=
MANE Select
|
ENSP00000281928.3:p.Gly1005=
|
|
ENST00000548743.2:c.2985G=
|
ENSP00000448553.2:p.Gly995=
|
|
ENST00000549786.2:c.2443G=
|
|
|
ENST00000648173.1:n.1810G=
|
|
|
ENST00000648379.1:n.1383G=
|
|
|
ENST00000648737.1:n.2779G=
|
|
|
ENST00000648916.1:n.1026G=
|
|
|
ENST00000649607.1:c.1199G=
|
|
|
ENST00000650226.1:c.3015G=
|
ENSP00000496981.1:p.Gly1005=
|
|
ENST00000281928.7:c.3015G=
|
ENSP00000281928.3:p.Gly1005=
|
|
NM_015335.4:c.3015G=
|
NP_056150.1:p.Gly1005=
|
|
XM_011538080.1:c.3015G=
|
XP_011536382.1:p.Gly1005=
|
|
XM_011538081.1:c.3012G=
|
XP_011536383.1:p.Gly1004=
|
|
XM_011538082.1:c.2985G=
|
XP_011536384.1:p.Gly995=
|
|
XM_011538080.2:c.3015G=
|
XP_011536382.1:p.Gly1005=
|
|
XM_011538081.2:c.3012G=
|
XP_011536383.1:p.Gly1004=
|
|
XM_011538082.2:c.2985G=
|
XP_011536384.1:p.Gly995=
|
|
XM_017019090.1:c.3012G=
|
XP_016874579.1:p.Gly1004=
|
|
NM_015335.5:c.3015G=
MANE Select
|
NP_056150.1:p.Gly1005=
|
|