ENST00000683611.1:n.1187C>G
|
|
|
ENST00000265104.5:c.13854C>G
MANE Select
|
ENSP00000265104.4:p.Ala4618=
|
|
ENST00000681290.1:c.13809C>G
|
ENSP00000505288.1:p.Ala4603=
|
|
ENST00000265104.4:c.13854C>G
|
ENSP00000265104.4:p.Ala4618=
|
|
NM_001369.2:c.13854C>G
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NP_001360.1:p.Ala4618=
|
|
XM_005248262.2:c.13809C>G
|
XP_005248319.1:p.Ala4603=
|
|
XM_005248262.3:c.13962C>G
|
XP_005248319.2:p.Ala4654=
|
|
XM_017009177.1:c.13542C>G
|
XP_016864666.1:p.Ala4514=
|
|
XM_017009178.1:c.12867C>G
|
XP_016864667.1:p.Ala4289=
|
|
XM_017009179.2:c.12867C>G
|
XP_016864668.1:p.Ala4289=
|
|
XM_017009185.1:c.9051C>G
|
XP_016864674.1:p.Ala3017=
|
|
XM_017009186.1:c.8604C>G
|
XP_016864675.1:p.Ala2868=
|
|
XM_017009188.1:c.7941C>G
|
XP_016864677.1:p.Ala2647=
|
|
XM_024454388.1:c.12867C>G
|
XP_024310156.1:p.Ala4289=
|
|
XM_024454389.1:c.12456C>G
|
XP_024310157.1:p.Ala4152=
|
|
NM_001369.3:c.13854C>G
MANE Select
|
NP_001360.1:p.Ala4618=
|
|