ENST00000683611.1:n.1071C>G
|
|
|
ENST00000265104.5:c.13738C>G
MANE Select
|
ENSP00000265104.4:p.Arg4580Gly
|
|
ENST00000681290.1:c.13693C>G
|
ENSP00000505288.1:p.Arg4565Gly
|
|
ENST00000265104.4:c.13738C>G
|
ENSP00000265104.4:p.Arg4580Gly
|
|
NM_001369.2:c.13738C>G
|
NP_001360.1:p.Arg4580Gly
|
|
XM_005248262.2:c.13693C>G
|
XP_005248319.1:p.Arg4565Gly
|
|
XM_005248262.3:c.13846C>G
|
XP_005248319.2:p.Arg4616Gly
|
|
XM_017009177.1:c.13426C>G
|
XP_016864666.1:p.Arg4476Gly
|
|
XM_017009178.1:c.12751C>G
|
XP_016864667.1:p.Arg4251Gly
|
|
XM_017009179.2:c.12751C>G
|
XP_016864668.1:p.Arg4251Gly
|
|
XM_017009185.1:c.8935C>G
|
XP_016864674.1:p.Arg2979Gly
|
|
XM_017009186.1:c.8488C>G
|
XP_016864675.1:p.Arg2830Gly
|
|
XM_017009188.1:c.7825C>G
|
XP_016864677.1:p.Arg2609Gly
|
|
XM_024454388.1:c.12751C>G
|
XP_024310156.1:p.Arg4251Gly
|
|
XM_024454389.1:c.12340C>G
|
XP_024310157.1:p.Arg4114Gly
|
|
NM_001369.3:c.13738C>G
MANE Select
|
NP_001360.1:p.Arg4580Gly
|
|