ENST00000318471.5:c.736A>G
MANE Select
|
ENSP00000315680.3:p.Arg246Gly
|
|
ENST00000541292.6:c.736A>G
|
ENSP00000441004.1:p.Arg246Gly
|
|
ENST00000678002.1:c.424A>G
|
|
|
ENST00000678557.1:c.622A>G
|
ENSP00000502962.1:p.Arg208Gly
|
|
ENST00000678593.1:c.741A>G
|
ENSP00000503841.1:n.741A>G
|
|
ENST00000679286.1:c.616A>G
|
ENSP00000503168.1:p.Arg206Gly
|
|
ENST00000318471.4:c.736A>G
|
ENSP00000315680.3:p.Arg246Gly
|
|
ENST00000541292.5:c.736A>G
|
ENSP00000441004.1:p.Arg246Gly
|
|
NM_000288.3:c.736A>G
|
NP_000279.1:p.Arg246Gly
|
|
XM_005267019.3:c.622A>G
|
XP_005267076.1:p.Arg208Gly
|
|
XM_006715502.1:c.442A>G
|
XP_006715565.1:p.Arg148Gly
|
|
XM_011535900.1:c.526+23811A>G
|
XP_011534202.1:n.526+23811A>G
|
|
XM_005267019.4:c.622A>G
|
XP_005267076.1:p.Arg208Gly
|
|
XM_006715502.2:c.442A>G
|
XP_006715565.1:p.Arg148Gly
|
|
XM_017010934.2:c.526+23811A>G
|
XP_016866423.1:n.526+23811A>G
|
|
NM_000288.4:c.736A>G
MANE Select
|
NP_000279.1:p.Arg246Gly
|
|