ENST00000683611.1:n.1194T>G
|
|
|
ENST00000265104.5:c.13861T>G
MANE Select
|
ENSP00000265104.4:p.Cys4621Gly
|
|
ENST00000681290.1:c.13816T>G
|
ENSP00000505288.1:p.Cys4606Gly
|
|
ENST00000265104.4:c.13861T>G
|
ENSP00000265104.4:p.Cys4621Gly
|
|
NM_001369.2:c.13861T>G
|
NP_001360.1:p.Cys4621Gly
|
|
XM_005248262.2:c.13816T>G
|
XP_005248319.1:p.Cys4606Gly
|
|
XM_005248262.3:c.13969T>G
|
XP_005248319.2:p.Cys4657Gly
|
|
XM_017009177.1:c.13549T>G
|
XP_016864666.1:p.Cys4517Gly
|
|
XM_017009178.1:c.12874T>G
|
XP_016864667.1:p.Cys4292Gly
|
|
XM_017009179.2:c.12874T>G
|
XP_016864668.1:p.Cys4292Gly
|
|
XM_017009185.1:c.9058T>G
|
XP_016864674.1:p.Cys3020Gly
|
|
XM_017009186.1:c.8611T>G
|
XP_016864675.1:p.Cys2871Gly
|
|
XM_017009188.1:c.7948T>G
|
XP_016864677.1:p.Cys2650Gly
|
|
XM_024454388.1:c.12874T>G
|
XP_024310156.1:p.Cys4292Gly
|
|
XM_024454389.1:c.12463T>G
|
XP_024310157.1:p.Cys4155Gly
|
|
NM_001369.3:c.13861T>G
MANE Select
|
NP_001360.1:p.Cys4621Gly
|
|