ENST00000262494.13:c.627C>A
|
ENSP00000262494.7:p.Arg209=
|
|
ENST00000262493.12:c.627C>A
MANE Select
|
ENSP00000262493.6:p.Arg209=
|
|
ENST00000262494.12:c.627C>A
|
ENSP00000262494.7:p.Arg209=
|
|
ENST00000562316.6:c.294C>A
|
ENSP00000457238.2:p.Arg98=
|
|
ENST00000568375.2:c.19C>A
|
|
|
ENST00000638185.1:n.842C>A
|
|
|
ENST00000638210.1:n.927C>A
|
|
|
ENST00000638705.1:c.627C>A
|
ENSP00000491223.1:p.Arg209=
|
|
ENST00000638836.1:n.537C>A
|
|
|
ENST00000639055.1:n.1348C>A
|
|
|
ENST00000639251.1:n.528C>A
|
|
|
ENST00000639268.1:c.262C>A
|
|
|
ENST00000639341.1:c.152C>A
|
|
|
ENST00000639770.1:c.665C>A
|
ENSP00000491999.1:n.665C>A
|
|
ENST00000640390.1:n.557C>A
|
|
|
ENST00000640560.1:n.403C>A
|
|
|
ENST00000640893.1:c.*25C>A
|
ENSP00000492677.1:n.*25C>A
|
|
ENST00000262493.10:c.627C>A
|
ENSP00000262493.6:p.Arg209=
|
|
ENST00000262494.11:c.627C>A
|
ENSP00000262494.7:p.Arg209=
|
|
ENST00000568375.1:n.19C>A
|
|
|
NM_020988.2:c.627C>A
|
NP_066268.1:p.Arg209=
|
|
NM_138736.2:c.627C>A
|
NP_620073.2:p.Arg209=
|
|
XM_011523003.1:c.501C>A
|
XP_011521305.1:p.Arg167=
|
|
XM_011523003.3:c.501C>A
|
XP_011521305.1:p.Arg167=
|
|
NM_020988.3:c.627C>A
MANE Select
|
NP_066268.1:p.Arg209=
|
|
NM_138736.3:c.627C>A
|
NP_620073.2:p.Arg209=
|
|