ENST00000683611.1:n.1081C>T
|
|
|
ENST00000265104.5:c.13748C>T
MANE Select
|
ENSP00000265104.4:p.Ser4583Phe
|
|
ENST00000681290.1:c.13703C>T
|
ENSP00000505288.1:p.Ser4568Phe
|
|
ENST00000265104.4:c.13748C>T
|
ENSP00000265104.4:p.Ser4583Phe
|
|
NM_001369.2:c.13748C>T
|
NP_001360.1:p.Ser4583Phe
|
|
XM_005248262.2:c.13703C>T
|
XP_005248319.1:p.Ser4568Phe
|
|
XM_005248262.3:c.13856C>T
|
XP_005248319.2:p.Ser4619Phe
|
|
XM_017009177.1:c.13436C>T
|
XP_016864666.1:p.Ser4479Phe
|
|
XM_017009178.1:c.12761C>T
|
XP_016864667.1:p.Ser4254Phe
|
|
XM_017009179.2:c.12761C>T
|
XP_016864668.1:p.Ser4254Phe
|
|
XM_017009185.1:c.8945C>T
|
XP_016864674.1:p.Ser2982Phe
|
|
XM_017009186.1:c.8498C>T
|
XP_016864675.1:p.Ser2833Phe
|
|
XM_017009188.1:c.7835C>T
|
XP_016864677.1:p.Ser2612Phe
|
|
XM_024454388.1:c.12761C>T
|
XP_024310156.1:p.Ser4254Phe
|
|
XM_024454389.1:c.12350C>T
|
XP_024310157.1:p.Ser4117Phe
|
|
NM_001369.3:c.13748C>T
MANE Select
|
NP_001360.1:p.Ser4583Phe
|
|