ENST00000265104.5:c.9394T>G
MANE Select
|
ENSP00000265104.4:p.Ser3132Ala
|
|
ENST00000681290.1:c.9349T>G
|
ENSP00000505288.1:p.Ser3117Ala
|
|
ENST00000265104.4:c.9394T>G
|
ENSP00000265104.4:p.Ser3132Ala
|
|
ENST00000504001.3:n.106T>G
|
|
|
NM_001369.2:c.9394T>G
|
NP_001360.1:p.Ser3132Ala
|
|
XM_005248262.2:c.9349T>G
|
XP_005248319.1:p.Ser3117Ala
|
|
XM_005248262.3:c.9502T>G
|
XP_005248319.2:p.Ser3168Ala
|
|
XM_017009177.1:c.9502T>G
|
XP_016864666.1:p.Ser3168Ala
|
|
XM_017009178.1:c.8407T>G
|
XP_016864667.1:p.Ser2803Ala
|
|
XM_017009179.2:c.8407T>G
|
XP_016864668.1:p.Ser2803Ala
|
|
XM_017009180.1:c.9502T>G
|
XP_016864669.1:p.Ser3168Ala
|
|
XM_017009181.1:c.9502T>G
|
XP_016864670.1:p.Ser3168Ala
|
|
XM_017009182.1:c.9502T>G
|
XP_016864671.1:p.Ser3168Ala
|
|
XM_017009183.1:c.9502T>G
|
XP_016864672.1:p.Ser3168Ala
|
|
XM_017009185.1:c.4591T>G
|
XP_016864674.1:p.Ser1531Ala
|
|
XM_017009186.1:c.4144T>G
|
XP_016864675.1:p.Ser1382Ala
|
|
XM_017009188.1:c.3481T>G
|
XP_016864677.1:p.Ser1161Ala
|
|
XM_024454388.1:c.8407T>G
|
XP_024310156.1:p.Ser2803Ala
|
|
XM_024454389.1:c.7996T>G
|
XP_024310157.1:p.Ser2666Ala
|
|
NM_001369.3:c.9394T>G
MANE Select
|
NP_001360.1:p.Ser3132Ala
|
|