ENST00000265104.5:c.10656C>G
MANE Select
|
ENSP00000265104.4:p.Ala3552=
|
|
ENST00000681290.1:c.10611C>G
|
ENSP00000505288.1:p.Ala3537=
|
|
ENST00000265104.4:c.10656C>G
|
ENSP00000265104.4:p.Ala3552=
|
|
NM_001369.2:c.10656C>G
|
NP_001360.1:p.Ala3552=
|
|
XM_005248262.2:c.10611C>G
|
XP_005248319.1:p.Ala3537=
|
|
XM_005248262.3:c.10764C>G
|
XP_005248319.2:p.Ala3588=
|
|
XM_017009177.1:c.10764C>G
|
XP_016864666.1:p.Ala3588=
|
|
XM_017009178.1:c.9669C>G
|
XP_016864667.1:p.Ala3223=
|
|
XM_017009179.2:c.9669C>G
|
XP_016864668.1:p.Ala3223=
|
|
XM_017009180.1:c.10764C>G
|
XP_016864669.1:p.Ala3588=
|
|
XM_017009181.1:c.10764C>G
|
XP_016864670.1:p.Ala3588=
|
|
XM_017009182.1:c.10764C>G
|
XP_016864671.1:p.Ala3588=
|
|
XM_017009185.1:c.5853C>G
|
XP_016864674.1:p.Ala1951=
|
|
XM_017009186.1:c.5406C>G
|
XP_016864675.1:p.Ala1802=
|
|
XM_017009188.1:c.4743C>G
|
XP_016864677.1:p.Ala1581=
|
|
XM_024454388.1:c.9669C>G
|
XP_024310156.1:p.Ala3223=
|
|
XM_024454389.1:c.9258C>G
|
XP_024310157.1:p.Ala3086=
|
|
NM_001369.3:c.10656C>G
MANE Select
|
NP_001360.1:p.Ala3552=
|
|