ENST00000265104.5:c.12602T>C
MANE Select
|
ENSP00000265104.4:p.Phe4201Ser
|
|
ENST00000681290.1:c.12557T>C
|
ENSP00000505288.1:p.Phe4186Ser
|
|
ENST00000265104.4:c.12602T>C
|
ENSP00000265104.4:p.Phe4201Ser
|
|
NM_001369.2:c.12602T>C
|
NP_001360.1:p.Phe4201Ser
|
|
XM_005248262.2:c.12557T>C
|
XP_005248319.1:p.Phe4186Ser
|
|
XM_005248262.3:c.12710T>C
|
XP_005248319.2:p.Phe4237Ser
|
|
XM_017009177.1:c.12710T>C
|
XP_016864666.1:p.Phe4237Ser
|
|
XM_017009178.1:c.11615T>C
|
XP_016864667.1:p.Phe3872Ser
|
|
XM_017009179.2:c.11615T>C
|
XP_016864668.1:p.Phe3872Ser
|
|
XM_017009180.1:c.12710T>C
|
XP_016864669.1:p.Phe4237Ser
|
|
XM_017009185.1:c.7799T>C
|
XP_016864674.1:p.Phe2600Ser
|
|
XM_017009186.1:c.7352T>C
|
XP_016864675.1:p.Phe2451Ser
|
|
XM_017009188.1:c.6689T>C
|
XP_016864677.1:p.Phe2230Ser
|
|
XM_024454388.1:c.11615T>C
|
XP_024310156.1:p.Phe3872Ser
|
|
XM_024454389.1:c.11204T>C
|
XP_024310157.1:p.Phe3735Ser
|
|
NM_001369.3:c.12602T>C
MANE Select
|
NP_001360.1:p.Phe4201Ser
|
|