ENST00000265104.5:c.11492C>G
MANE Select
|
ENSP00000265104.4:p.Thr3831Ser
|
|
ENST00000681290.1:c.11447C>G
|
ENSP00000505288.1:p.Thr3816Ser
|
|
ENST00000265104.4:c.11492C>G
|
ENSP00000265104.4:p.Thr3831Ser
|
|
NM_001369.2:c.11492C>G
|
NP_001360.1:p.Thr3831Ser
|
|
XM_005248262.2:c.11447C>G
|
XP_005248319.1:p.Thr3816Ser
|
|
XM_005248262.3:c.11600C>G
|
XP_005248319.2:p.Thr3867Ser
|
|
XM_017009177.1:c.11600C>G
|
XP_016864666.1:p.Thr3867Ser
|
|
XM_017009178.1:c.10505C>G
|
XP_016864667.1:p.Thr3502Ser
|
|
XM_017009179.2:c.10505C>G
|
XP_016864668.1:p.Thr3502Ser
|
|
XM_017009180.1:c.11600C>G
|
XP_016864669.1:p.Thr3867Ser
|
|
XM_017009181.1:c.11600C>G
|
XP_016864670.1:p.Thr3867Ser
|
|
XM_017009182.1:c.11356C>G
|
XP_016864671.1:p.Leu3786Val
|
|
XM_017009185.1:c.6689C>G
|
XP_016864674.1:p.Thr2230Ser
|
|
XM_017009186.1:c.6242C>G
|
XP_016864675.1:p.Thr2081Ser
|
|
XM_017009188.1:c.5579C>G
|
XP_016864677.1:p.Thr1860Ser
|
|
XM_024454388.1:c.10505C>G
|
XP_024310156.1:p.Thr3502Ser
|
|
XM_024454389.1:c.10094C>G
|
XP_024310157.1:p.Thr3365Ser
|
|
NM_001369.3:c.11492C>G
MANE Select
|
NP_001360.1:p.Thr3831Ser
|
|