ENST00000449082.3:c.4873G>A
MANE Select
|
ENSP00000390600.2:p.Gly1625Ser
|
|
ENST00000643924.1:c.4870G>A
|
ENSP00000495595.1:p.Gly1624Ser
|
|
ENST00000655275.1:c.4897G>A
|
ENSP00000499510.1:p.Gly1633Ser
|
|
ENST00000449082.2:c.4873G>A
|
ENSP00000390600.2:p.Gly1625Ser
|
|
NM_001293306.2:c.4870G>A
|
NP_001280235.2:p.Gly1624Ser
|
|
NM_001293307.2:c.4579G>A
|
NP_001280236.2:p.Gly1527Ser
|
|
NM_006514.3:c.4873G>A
|
NP_006505.3:p.Gly1625Ser
|
|
XM_005265371.2:c.4882G>A
|
XP_005265428.1:p.Gly1628Ser
|
|
XM_011533993.1:c.4879G>A
|
XP_011532295.1:p.Gly1627Ser
|
|
XM_011533994.1:c.4588G>A
|
XP_011532296.1:p.Gly1530Ser
|
|
XM_005265371.3:c.4882G>A
|
XP_005265428.1:p.Gly1628Ser
|
|
XM_011533993.2:c.4879G>A
|
XP_011532295.1:p.Gly1627Ser
|
|
XM_011533994.2:c.4588G>A
|
XP_011532296.1:p.Gly1530Ser
|
|
NM_006514.4:c.4873G>A
MANE Select
|
NP_006505.4:p.Gly1625Ser
|
|