ENST00000265104.5:c.11552T>G
MANE Select
|
ENSP00000265104.4:p.Phe3851Cys
|
|
ENST00000681290.1:c.11507T>G
|
ENSP00000505288.1:p.Phe3836Cys
|
|
ENST00000265104.4:c.11552T>G
|
ENSP00000265104.4:p.Phe3851Cys
|
|
NM_001369.2:c.11552T>G
|
NP_001360.1:p.Phe3851Cys
|
|
XM_005248262.2:c.11507T>G
|
XP_005248319.1:p.Phe3836Cys
|
|
XM_005248262.3:c.11660T>G
|
XP_005248319.2:p.Phe3887Cys
|
|
XM_017009177.1:c.11660T>G
|
XP_016864666.1:p.Phe3887Cys
|
|
XM_017009178.1:c.10565T>G
|
XP_016864667.1:p.Phe3522Cys
|
|
XM_017009179.2:c.10565T>G
|
XP_016864668.1:p.Phe3522Cys
|
|
XM_017009180.1:c.11660T>G
|
XP_016864669.1:p.Phe3887Cys
|
|
XM_017009181.1:c.11660T>G
|
XP_016864670.1:p.Phe3887Cys
|
|
XM_017009182.1:c.11416T>G
|
XP_016864671.1:p.Leu3806Val
|
|
XM_017009185.1:c.6749T>G
|
XP_016864674.1:p.Phe2250Cys
|
|
XM_017009186.1:c.6302T>G
|
XP_016864675.1:p.Phe2101Cys
|
|
XM_017009188.1:c.5639T>G
|
XP_016864677.1:p.Phe1880Cys
|
|
XM_024454388.1:c.10565T>G
|
XP_024310156.1:p.Phe3522Cys
|
|
XM_024454389.1:c.10154T>G
|
XP_024310157.1:p.Phe3385Cys
|
|
NM_001369.3:c.11552T>G
MANE Select
|
NP_001360.1:p.Phe3851Cys
|
|