ENST00000367049.9:c.6348G>A
MANE Select
|
ENSP00000356016.4:p.Gln2116=
|
|
ENST00000367051.6:c.4998G>A
|
ENSP00000356018.1:p.Gln1666=
|
|
ENST00000367052.6:c.4998G>A
|
ENSP00000356019.1:p.Gln1666=
|
|
ENST00000367053.6:c.4998G>A
|
ENSP00000356020.1:p.Gln1666=
|
|
ENST00000400960.7:c.4998G>A
|
ENSP00000383744.2:p.Gln1666=
|
|
ENST00000367049.8:c.6348G>A
|
ENSP00000356016.4:p.Gln2116=
|
|
ENST00000367051.5:c.4998G>A
|
ENSP00000356018.1:p.Gln1666=
|
|
ENST00000367052.5:c.4998G>A
|
ENSP00000356019.1:p.Gln1666=
|
|
ENST00000367053.5:c.4998G>A
|
ENSP00000356020.1:p.Gln1666=
|
|
ENST00000400960.6:c.4998G>A
|
ENSP00000383744.2:p.Gln1666=
|
|
ENST00000529814.1:c.1180-4846G>A
|
|
|
NM_000573.3:c.4998G>A
|
NP_000564.2:p.Gln1666=
|
|
NM_000651.4:c.6348G>A
|
NP_000642.3:p.Gln2116=
|
|
XM_006711166.2:c.6363G>A
|
XP_006711229.1:p.Gln2121=
|
|
XM_011509205.1:c.6363G>A
|
XP_011507507.1:p.Gln2121=
|
|
NM_000651.5:c.6348G>A
|
NP_000642.3:p.Gln2116=
|
|
XM_024453287.1:c.5013G>A
|
XP_024309055.1:p.Gln1671=
|
|
NM_000573.4:c.4998G>A
|
NP_000564.2:p.Gln1666=
|
|
NM_000651.6:c.6348G>A
MANE Select
|
NP_000642.3:p.Gln2116=
|
|