ENST00000265104.5:c.10601T>A
MANE Select
|
ENSP00000265104.4:p.Phe3534Tyr
|
|
ENST00000681290.1:c.10556T>A
|
ENSP00000505288.1:p.Phe3519Tyr
|
|
ENST00000265104.4:c.10601T>A
|
ENSP00000265104.4:p.Phe3534Tyr
|
|
NM_001369.2:c.10601T>A
|
NP_001360.1:p.Phe3534Tyr
|
|
XM_005248262.2:c.10556T>A
|
XP_005248319.1:p.Phe3519Tyr
|
|
XM_005248262.3:c.10709T>A
|
XP_005248319.2:p.Phe3570Tyr
|
|
XM_017009177.1:c.10709T>A
|
XP_016864666.1:p.Phe3570Tyr
|
|
XM_017009178.1:c.9614T>A
|
XP_016864667.1:p.Phe3205Tyr
|
|
XM_017009179.2:c.9614T>A
|
XP_016864668.1:p.Phe3205Tyr
|
|
XM_017009180.1:c.10709T>A
|
XP_016864669.1:p.Phe3570Tyr
|
|
XM_017009181.1:c.10709T>A
|
XP_016864670.1:p.Phe3570Tyr
|
|
XM_017009182.1:c.10709T>A
|
XP_016864671.1:p.Phe3570Tyr
|
|
XM_017009185.1:c.5798T>A
|
XP_016864674.1:p.Phe1933Tyr
|
|
XM_017009186.1:c.5351T>A
|
XP_016864675.1:p.Phe1784Tyr
|
|
XM_017009188.1:c.4688T>A
|
XP_016864677.1:p.Phe1563Tyr
|
|
XM_024454388.1:c.9614T>A
|
XP_024310156.1:p.Phe3205Tyr
|
|
XM_024454389.1:c.9203T>A
|
XP_024310157.1:p.Phe3068Tyr
|
|
NM_001369.3:c.10601T>A
MANE Select
|
NP_001360.1:p.Phe3534Tyr
|
|