ENST00000265104.5:c.11507T>C
MANE Select
|
ENSP00000265104.4:p.Val3836Ala
|
|
ENST00000681290.1:c.11462T>C
|
ENSP00000505288.1:p.Val3821Ala
|
|
ENST00000265104.4:c.11507T>C
|
ENSP00000265104.4:p.Val3836Ala
|
|
NM_001369.2:c.11507T>C
|
NP_001360.1:p.Val3836Ala
|
|
XM_005248262.2:c.11462T>C
|
XP_005248319.1:p.Val3821Ala
|
|
XM_005248262.3:c.11615T>C
|
XP_005248319.2:p.Val3872Ala
|
|
XM_017009177.1:c.11615T>C
|
XP_016864666.1:p.Val3872Ala
|
|
XM_017009178.1:c.10520T>C
|
XP_016864667.1:p.Val3507Ala
|
|
XM_017009179.2:c.10520T>C
|
XP_016864668.1:p.Val3507Ala
|
|
XM_017009180.1:c.11615T>C
|
XP_016864669.1:p.Val3872Ala
|
|
XM_017009181.1:c.11615T>C
|
XP_016864670.1:p.Val3872Ala
|
|
XM_017009182.1:c.11371T>C
|
XP_016864671.1:p.Leu3791=
|
|
XM_017009185.1:c.6704T>C
|
XP_016864674.1:p.Val2235Ala
|
|
XM_017009186.1:c.6257T>C
|
XP_016864675.1:p.Val2086Ala
|
|
XM_017009188.1:c.5594T>C
|
XP_016864677.1:p.Val1865Ala
|
|
XM_024454388.1:c.10520T>C
|
XP_024310156.1:p.Val3507Ala
|
|
XM_024454389.1:c.10109T>C
|
XP_024310157.1:p.Val3370Ala
|
|
NM_001369.3:c.11507T>C
MANE Select
|
NP_001360.1:p.Val3836Ala
|
|