ENST00000247933.9:c.1284G>A
|
ENSP00000247933.4:p.Gln428=
|
|
ENST00000514224.2:c.1284G>A
MANE Select
|
ENSP00000425081.2:p.Gln428=
|
|
ENST00000652070.1:n.1340G>A
|
|
|
ENST00000247933.8:c.1284G>A
|
ENSP00000247933.4:p.Gln428=
|
|
ENST00000502829.1:n.86G>A
|
|
|
ENST00000514224.1:c.888G>A
|
ENSP00000425081.1:p.Gln296=
|
|
ENST00000514698.5:n.1391G>A
|
|
|
NM_000203.4:c.1284G>A
|
NP_000194.2:p.Gln428=
|
|
NR_110313.1:n.1372G>A
|
|
|
XM_006713882.2:c.888G>A
|
XP_006713945.1:p.Gln296=
|
|
XM_011513459.1:c.1350G>A
|
XP_011511761.1:p.Gln450=
|
|
XM_011513460.1:c.1143G>A
|
XP_011511762.1:p.Gln381=
|
|
XM_011513461.1:c.1077G>A
|
XP_011511763.1:p.Gln359=
|
|
XM_011513462.1:c.996G>A
|
XP_011511764.1:p.Gln332=
|
|
XM_011513463.1:c.996G>A
|
XP_011511765.1:p.Gln332=
|
|
XR_924947.1:n.1353G>A
|
|
|
NM_000203.5:c.1284G>A
MANE Select
|
NP_000194.2:p.Gln428=
|
|
NM_001363576.1:c.888G>A
|
NP_001350505.1:p.Gln296=
|
|
XM_011513461.2:c.1077G>A
|
XP_011511763.1:p.Gln359=
|
|
XM_017008163.1:c.324G>A
|
XP_016863652.1:p.Gln108=
|
|