NM_004482.4:c.677C=
MANE Select
|
NP_004473.2:p.Ala226=
|
ENST00000392701.8:c.677C=
MANE Select
|
ENSP00000376465.3:p.Ala226=
|
NM_004482.3:c.677C=
|
NP_004473.2:p.Ala226=
|
ENST00000392701.7:c.677C=
|
ENSP00000376465.3:p.Ala226=
|
ENST00000412248.5:c.677C=
|
ENSP00000412643.1:p.Ala226=
|
ENST00000437849.1:c.65C=
|
ENSP00000391104.1:p.Ala22=
|
XM_005246449.1:c.677C=
|
XP_005246506.1:p.Ala226=
|
XM_006712402.2:c.677C=
|
XP_006712465.1:p.Ala226=
|
XM_011510929.1:c.677C=
|
XP_011509231.1:p.Ala226=
|
XM_017003770.1:c.677C=
|
XP_016859259.1:p.Ala226=
|
XR_002959253.1:n.1018C=
|
|