ENST00000683611.1:n.554C>G
|
|
|
ENST00000265104.5:c.13221C>G
MANE Select
|
ENSP00000265104.4:p.Val4407=
|
|
ENST00000681290.1:c.13176C>G
|
ENSP00000505288.1:p.Val4392=
|
|
ENST00000265104.4:c.13221C>G
|
ENSP00000265104.4:p.Val4407=
|
|
NM_001369.2:c.13221C>G
|
NP_001360.1:p.Val4407=
|
|
XM_005248262.2:c.13176C>G
|
XP_005248319.1:p.Val4392=
|
|
XM_005248262.3:c.13329C>G
|
XP_005248319.2:p.Val4443=
|
|
XM_017009177.1:c.12909C>G
|
XP_016864666.1:p.Val4303=
|
|
XM_017009178.1:c.12234C>G
|
XP_016864667.1:p.Val4078=
|
|
XM_017009179.2:c.12234C>G
|
XP_016864668.1:p.Val4078=
|
|
XM_017009185.1:c.8418C>G
|
XP_016864674.1:p.Val2806=
|
|
XM_017009186.1:c.7971C>G
|
XP_016864675.1:p.Val2657=
|
|
XM_017009188.1:c.7308C>G
|
XP_016864677.1:p.Val2436=
|
|
XM_024454388.1:c.12234C>G
|
XP_024310156.1:p.Val4078=
|
|
XM_024454389.1:c.11823C>G
|
XP_024310157.1:p.Val3941=
|
|
NM_001369.3:c.13221C>G
MANE Select
|
NP_001360.1:p.Val4407=
|
|