ENST00000683611.1:n.819C>G
|
|
|
ENST00000265104.5:c.13486C>G
MANE Select
|
ENSP00000265104.4:p.Arg4496Gly
|
|
ENST00000681290.1:c.13441C>G
|
ENSP00000505288.1:p.Arg4481Gly
|
|
ENST00000265104.4:c.13486C>G
|
ENSP00000265104.4:p.Arg4496Gly
|
|
NM_001369.2:c.13486C>G
|
NP_001360.1:p.Arg4496Gly
|
|
XM_005248262.2:c.13441C>G
|
XP_005248319.1:p.Arg4481Gly
|
|
XM_005248262.3:c.13594C>G
|
XP_005248319.2:p.Arg4532Gly
|
|
XM_017009177.1:c.13174C>G
|
XP_016864666.1:p.Arg4392Gly
|
|
XM_017009178.1:c.12499C>G
|
XP_016864667.1:p.Arg4167Gly
|
|
XM_017009179.2:c.12499C>G
|
XP_016864668.1:p.Arg4167Gly
|
|
XM_017009185.1:c.8683C>G
|
XP_016864674.1:p.Arg2895Gly
|
|
XM_017009186.1:c.8236C>G
|
XP_016864675.1:p.Arg2746Gly
|
|
XM_017009188.1:c.7573C>G
|
XP_016864677.1:p.Arg2525Gly
|
|
XM_024454388.1:c.12499C>G
|
XP_024310156.1:p.Arg4167Gly
|
|
XM_024454389.1:c.12088C>G
|
XP_024310157.1:p.Arg4030Gly
|
|
NM_001369.3:c.13486C>G
MANE Select
|
NP_001360.1:p.Arg4496Gly
|
|