ENST00000389857.11:c.5089A>G
MANE Select
|
ENSP00000374507.6:p.Ser1697Gly
|
|
ENST00000331194.8:c.661A>G
|
ENSP00000330332.8:p.Ser221Gly
|
|
ENST00000334448.5:n.901A>G
|
|
|
ENST00000389857.10:c.5089A>G
|
ENSP00000374507.6:p.Ser1697Gly
|
|
ENST00000556726.5:c.1317A>G
|
|
|
NM_001080414.3:c.5089A>G
|
NP_001073883.2:p.Ser1697Gly
|
|
XM_011536796.1:c.4981A>G
|
XP_011535098.1:p.Ser1661Gly
|
|
XR_429316.2:n.5364A>G
|
|
|
XM_011536796.2:c.4981A>G
|
XP_011535098.1:p.Ser1661Gly
|
|
XM_017021336.1:c.2170A>G
|
XP_016876825.1:p.Ser724Gly
|
|
XR_429316.4:n.5362A>G
|
|
|
NM_001080414.4:c.5089A>G
MANE Select
|
NP_001073883.2:p.Ser1697Gly
|
|