ENST00000236850.5:c.597C=
MANE Select
|
ENSP00000236850.3:p.Ala199=
|
|
ENST00000236850.4:c.597C=
|
ENSP00000236850.3:p.Ala199=
|
|
ENST00000359492.6:c.597C=
|
ENSP00000352471.2:p.Ala199=
|
|
ENST00000375320.5:c.597C=
|
ENSP00000364469.1:p.Ala199=
|
|
ENST00000375323.5:c.597C=
|
ENSP00000364472.1:p.Ala199=
|
|
ENST00000375329.6:c.531C=
|
ENSP00000364478.2:p.Ala177=
|
|
NM_000039.1:c.597C= , LRG_767t1:c.597C=
|
NP_000030.1:p.Ala199=
|
|
XM_005271539.2:c.597C=
|
XP_005271596.1:p.Ala199=
|
|
XM_005271540.1:c.597C=
|
XP_005271597.1:p.Ala199=
|
|
NM_000039.2:c.597C=
|
NP_000030.1:p.Ala199=
|
|
NM_001318017.1:c.597C=
|
NP_001304946.1:p.Ala199=
|
|
NM_001318018.1:c.597C=
|
NP_001304947.1:p.Ala199=
|
|
NM_001318021.1:c.270C=
|
NP_001304950.1:p.Ala90=
|
|
NM_001318017.2:c.597C=
|
NP_001304946.1:p.Ala199=
|
|
NM_001318018.2:c.597C=
|
NP_001304947.1:p.Ala199=
|
|
NM_000039.3:c.597C=
MANE Select
|
NP_000030.1:p.Ala199=
|
|