ENST00000318471.5:c.752C>G
MANE Select
|
ENSP00000315680.3:p.Ser251Ter
|
|
ENST00000541292.6:c.*17C>G
|
ENSP00000441004.1:n.*17C>G
|
|
ENST00000678002.1:c.440C>G
|
|
|
ENST00000678557.1:c.638C>G
|
ENSP00000502962.1:p.Ser213Ter
|
|
ENST00000678593.1:c.757C>G
|
ENSP00000503841.1:n.757C>G
|
|
ENST00000679286.1:c.632C>G
|
ENSP00000503168.1:p.Ser211Ter
|
|
ENST00000318471.4:c.752C>G
|
ENSP00000315680.3:p.Ser251Ter
|
|
NM_000288.3:c.752C>G
|
NP_000279.1:p.Ser251Ter
|
|
XM_005267019.3:c.638C>G
|
XP_005267076.1:p.Ser213Ter
|
|
XM_006715502.1:c.458C>G
|
XP_006715565.1:p.Ser153Ter
|
|
XM_011535900.1:c.527-25940C>G
|
XP_011534202.1:n.527-25940C>G
|
|
XM_005267019.4:c.638C>G
|
XP_005267076.1:p.Ser213Ter
|
|
XM_006715502.2:c.458C>G
|
XP_006715565.1:p.Ser153Ter
|
|
XM_017010934.2:c.527-25940C>G
|
XP_016866423.1:n.527-25940C>G
|
|
NM_000288.4:c.752C>G
MANE Select
|
NP_000279.1:p.Ser251Ter
|
|