ENST00000265104.5:c.9827A>T
MANE Select
|
ENSP00000265104.4:p.Asp3276Val
|
|
ENST00000681290.1:c.9782A>T
|
ENSP00000505288.1:p.Asp3261Val
|
|
ENST00000265104.4:c.9827A>T
|
ENSP00000265104.4:p.Asp3276Val
|
|
ENST00000504001.3:n.539A>T
|
|
|
NM_001369.2:c.9827A>T
|
NP_001360.1:p.Asp3276Val
|
|
XM_005248262.2:c.9782A>T
|
XP_005248319.1:p.Asp3261Val
|
|
XM_005248262.3:c.9935A>T
|
XP_005248319.2:p.Asp3312Val
|
|
XM_017009177.1:c.9935A>T
|
XP_016864666.1:p.Asp3312Val
|
|
XM_017009178.1:c.8840A>T
|
XP_016864667.1:p.Asp2947Val
|
|
XM_017009179.2:c.8840A>T
|
XP_016864668.1:p.Asp2947Val
|
|
XM_017009180.1:c.9935A>T
|
XP_016864669.1:p.Asp3312Val
|
|
XM_017009181.1:c.9935A>T
|
XP_016864670.1:p.Asp3312Val
|
|
XM_017009182.1:c.9935A>T
|
XP_016864671.1:p.Asp3312Val
|
|
XM_017009185.1:c.5024A>T
|
XP_016864674.1:p.Asp1675Val
|
|
XM_017009186.1:c.4577A>T
|
XP_016864675.1:p.Asp1526Val
|
|
XM_017009188.1:c.3914A>T
|
XP_016864677.1:p.Asp1305Val
|
|
XM_024454388.1:c.8840A>T
|
XP_024310156.1:p.Asp2947Val
|
|
XM_024454389.1:c.8429A>T
|
XP_024310157.1:p.Asp2810Val
|
|
NM_001369.3:c.9827A>T
MANE Select
|
NP_001360.1:p.Asp3276Val
|
|