ENST00000265104.5:c.10988T>C
MANE Select
|
ENSP00000265104.4:p.Val3663Ala
|
|
ENST00000681290.1:c.10943T>C
|
ENSP00000505288.1:p.Val3648Ala
|
|
ENST00000265104.4:c.10988T>C
|
ENSP00000265104.4:p.Val3663Ala
|
|
NM_001369.2:c.10988T>C
|
NP_001360.1:p.Val3663Ala
|
|
XM_005248262.2:c.10943T>C
|
XP_005248319.1:p.Val3648Ala
|
|
XM_005248262.3:c.11096T>C
|
XP_005248319.2:p.Val3699Ala
|
|
XM_017009177.1:c.11096T>C
|
XP_016864666.1:p.Val3699Ala
|
|
XM_017009178.1:c.10001T>C
|
XP_016864667.1:p.Val3334Ala
|
|
XM_017009179.2:c.10001T>C
|
XP_016864668.1:p.Val3334Ala
|
|
XM_017009180.1:c.11096T>C
|
XP_016864669.1:p.Val3699Ala
|
|
XM_017009181.1:c.11096T>C
|
XP_016864670.1:p.Val3699Ala
|
|
XM_017009182.1:c.11096T>C
|
XP_016864671.1:p.Val3699Ala
|
|
XM_017009185.1:c.6185T>C
|
XP_016864674.1:p.Val2062Ala
|
|
XM_017009186.1:c.5738T>C
|
XP_016864675.1:p.Val1913Ala
|
|
XM_017009188.1:c.5075T>C
|
XP_016864677.1:p.Val1692Ala
|
|
XM_024454388.1:c.10001T>C
|
XP_024310156.1:p.Val3334Ala
|
|
XM_024454389.1:c.9590T>C
|
XP_024310157.1:p.Val3197Ala
|
|
NM_001369.3:c.10988T>C
MANE Select
|
NP_001360.1:p.Val3663Ala
|
|