ENST00000699485.1:c.990C>T
|
ENSP00000514396.1:p.Arg330=
|
|
ENST00000362057.4:c.2646C>T
MANE Select
|
ENSP00000354623.3:p.Arg882=
|
|
ENST00000674036.8:c.1619C>T
|
|
|
ENST00000674048.1:n.2527C>T
|
|
|
ENST00000265134.10:c.1497C>T
|
ENSP00000265134.6:p.Arg499=
|
|
ENST00000362057.3:c.2646C>T
|
ENSP00000354623.3:p.Arg882=
|
|
ENST00000374059.7:c.1593C>T
|
ENSP00000363172.3:p.Arg531=
|
|
NM_001083885.2:c.1497C>T
|
NP_001077354.2:p.Arg499=
|
|
NM_001173425.1:c.2643C>T
|
NP_001166896.1:p.Arg881=
|
|
NM_015404.3:c.2646C>T
|
NP_056219.3:p.Arg882=
|
|
XM_005251897.3:c.1983C>T
|
XP_005251954.2:p.Arg661=
|
|
XM_011518484.1:c.2679C>T
|
XP_011516786.1:p.Arg893=
|
|
XM_011518485.1:c.2679C>T
|
XP_011516787.1:p.Arg893=
|
|
XM_011518486.1:c.2676C>T
|
XP_011516788.1:p.Arg892=
|
|
XM_011518487.1:c.2553C>T
|
XP_011516789.1:p.Arg851=
|
|
XM_011518488.1:c.2436C>T
|
XP_011516790.1:p.Arg812=
|
|
XM_011518495.1:c.1356C>T
|
XP_011516797.1:p.Arg452=
|
|
NM_001346890.1:c.1593C>T
|
NP_001333819.1:p.Arg531=
|
|
XM_011518486.2:c.2676C>T
|
XP_011516788.1:p.Arg892=
|
|
XM_011518487.2:c.2553C>T
|
XP_011516789.1:p.Arg851=
|
|
XM_011518488.2:c.2436C>T
|
XP_011516790.1:p.Arg812=
|
|
NM_015404.4:c.2646C>T
MANE Select
|
NP_056219.3:p.Arg882=
|
|
NM_001173425.2:c.2643C>T
|
NP_001166896.1:p.Arg881=
|
|
NM_001083885.3:c.1497C>T
|
NP_001077354.2:p.Arg499=
|
|