ENST00000265104.5:c.9500T>G
MANE Select
|
ENSP00000265104.4:p.Phe3167Cys
|
|
ENST00000681290.1:c.9455T>G
|
ENSP00000505288.1:p.Phe3152Cys
|
|
ENST00000265104.4:c.9500T>G
|
ENSP00000265104.4:p.Phe3167Cys
|
|
ENST00000504001.3:n.212T>G
|
|
|
NM_001369.2:c.9500T>G
|
NP_001360.1:p.Phe3167Cys
|
|
XM_005248262.2:c.9455T>G
|
XP_005248319.1:p.Phe3152Cys
|
|
XM_005248262.3:c.9608T>G
|
XP_005248319.2:p.Phe3203Cys
|
|
XM_017009177.1:c.9608T>G
|
XP_016864666.1:p.Phe3203Cys
|
|
XM_017009178.1:c.8513T>G
|
XP_016864667.1:p.Phe2838Cys
|
|
XM_017009179.2:c.8513T>G
|
XP_016864668.1:p.Phe2838Cys
|
|
XM_017009180.1:c.9608T>G
|
XP_016864669.1:p.Phe3203Cys
|
|
XM_017009181.1:c.9608T>G
|
XP_016864670.1:p.Phe3203Cys
|
|
XM_017009182.1:c.9608T>G
|
XP_016864671.1:p.Phe3203Cys
|
|
XM_017009183.1:c.9608T>G
|
XP_016864672.1:p.Phe3203Cys
|
|
XM_017009185.1:c.4697T>G
|
XP_016864674.1:p.Phe1566Cys
|
|
XM_017009186.1:c.4250T>G
|
XP_016864675.1:p.Phe1417Cys
|
|
XM_017009188.1:c.3587T>G
|
XP_016864677.1:p.Phe1196Cys
|
|
XM_024454388.1:c.8513T>G
|
XP_024310156.1:p.Phe2838Cys
|
|
XM_024454389.1:c.8102T>G
|
XP_024310157.1:p.Phe2701Cys
|
|
NM_001369.3:c.9500T>G
MANE Select
|
NP_001360.1:p.Phe3167Cys
|
|