ENST00000264731.8:c.1748A>G
MANE Select
|
ENSP00000264731.3:p.Asp583Gly
|
|
ENST00000354600.10:c.1466A>G
MANE Plus Clinical
|
ENSP00000346614.5:p.Asp489Gly
|
|
ENST00000264731.7:c.1748A>G
|
ENSP00000264731.3:p.Asp583Gly
|
|
ENST00000320472.9:c.1509A>G
|
ENSP00000317510.5:p.Arg503=
|
|
ENST00000354600.9:c.1466A>G
|
ENSP00000346614.5:p.Asp489Gly
|
|
ENST00000392460.7:c.1654A>G
|
ENSP00000376253.3:p.Ile552Val
|
|
ENST00000392461.7:c.1227A>G
|
ENSP00000376254.3:p.Arg409=
|
|
ENST00000392463.6:c.1372A>G
|
ENSP00000376256.2:p.Ile458Val
|
|
ENST00000440651.6:c.1736A>G
|
ENSP00000394337.2:p.Asp579Gly
|
|
ENST00000449992.5:c.1211A>G
|
ENSP00000387839.1:p.Asp404Gly
|
|
ENST00000456148.1:c.1454A>G
|
ENSP00000389485.1:p.Asp485Gly
|
|
NM_001114978.1:c.1654A>G
|
NP_001108450.1:p.Ile552Val
|
|
NM_001114980.1:c.1466A>G
|
NP_001108452.1:p.Asp489Gly
|
|
NM_001114981.1:c.1372A>G
|
NP_001108453.1:p.Ile458Val
|
|
NM_003722.4:c.1748A>G
|
NP_003713.3:p.Asp583Gly
|
|
XM_005247843.2:c.1736A>G
|
XP_005247900.1:p.Asp579Gly
|
|
XM_005247844.3:c.1697A>G
|
XP_005247901.1:p.Asp566Gly
|
|
XM_011513251.1:c.1745A>G
|
XP_011511553.1:p.Asp582Gly
|
|
XM_011513252.1:c.1742A>G
|
XP_011511554.1:p.Asp581Gly
|
|
XM_011513253.1:c.1709A>G
|
XP_011511555.1:p.Asp570Gly
|
|
NM_001329144.1:c.1509A>G
|
NP_001316073.1:p.Arg503=
|
|
NM_001329145.1:c.1227A>G
|
NP_001316074.1:p.Arg409=
|
|
NM_001329146.1:c.1211A>G
|
NP_001316075.1:p.Asp404Gly
|
|
NM_001329148.1:c.1736A>G
|
NP_001316077.1:p.Asp579Gly
|
|
NM_001329149.1:c.1215A>G
|
NP_001316078.1:p.Arg405=
|
|
NM_001329150.1:c.960A>G
|
NP_001316079.1:p.Arg320=
|
|
NM_001329964.1:c.1742A>G
|
NP_001316893.1:p.Asp581Gly
|
|
NM_003722.5:c.1748A>G
MANE Select
|
NP_003713.3:p.Asp583Gly
|
|
NM_001114978.2:c.1654A>G
|
NP_001108450.1:p.Ile552Val
|
|
NM_001114980.2:c.1466A>G
MANE Plus Clinical
|
NP_001108452.1:p.Asp489Gly
|
|
NM_001114981.2:c.1372A>G
|
NP_001108453.1:p.Ile458Val
|
|
NM_001329144.2:c.1509A>G
|
NP_001316073.1:p.Arg503=
|
|
NM_001329145.2:c.1227A>G
|
NP_001316074.1:p.Arg409=
|
|
NM_001329146.2:c.1211A>G
|
NP_001316075.1:p.Asp404Gly
|
|
NM_001329148.2:c.1736A>G
|
NP_001316077.1:p.Asp579Gly
|
|
NM_001329149.2:c.1215A>G
|
NP_001316078.1:p.Arg405=
|
|
NM_001329150.2:c.960A>G
|
NP_001316079.1:p.Arg320=
|
|
NM_001329964.2:c.1742A>G
|
NP_001316893.1:p.Asp581Gly
|
|