ENST00000683611.1:n.490T>A
|
|
|
ENST00000265104.5:c.13157T>A
MANE Select
|
ENSP00000265104.4:p.Phe4386Tyr
|
|
ENST00000681290.1:c.13112T>A
|
ENSP00000505288.1:p.Phe4371Tyr
|
|
ENST00000265104.4:c.13157T>A
|
ENSP00000265104.4:p.Phe4386Tyr
|
|
NM_001369.2:c.13157T>A
|
NP_001360.1:p.Phe4386Tyr
|
|
XM_005248262.2:c.13112T>A
|
XP_005248319.1:p.Phe4371Tyr
|
|
XM_005248262.3:c.13265T>A
|
XP_005248319.2:p.Phe4422Tyr
|
|
XM_017009177.1:c.12845T>A
|
XP_016864666.1:p.Phe4282Tyr
|
|
XM_017009178.1:c.12170T>A
|
XP_016864667.1:p.Phe4057Tyr
|
|
XM_017009179.2:c.12170T>A
|
XP_016864668.1:p.Phe4057Tyr
|
|
XM_017009185.1:c.8354T>A
|
XP_016864674.1:p.Phe2785Tyr
|
|
XM_017009186.1:c.7907T>A
|
XP_016864675.1:p.Phe2636Tyr
|
|
XM_017009188.1:c.7244T>A
|
XP_016864677.1:p.Phe2415Tyr
|
|
XM_024454388.1:c.12170T>A
|
XP_024310156.1:p.Phe4057Tyr
|
|
XM_024454389.1:c.11759T>A
|
XP_024310157.1:p.Phe3920Tyr
|
|
NM_001369.3:c.13157T>A
MANE Select
|
NP_001360.1:p.Phe4386Tyr
|
|