ENST00000528025.6:c.13627G>A
|
ENSP00000437303.2:p.Ala4543Thr
|
|
ENST00000685198.1:c.13546G>A
|
ENSP00000510528.1:p.Ala4516Thr
|
|
ENST00000687971.1:c.13213G>A
|
ENSP00000510788.1:p.Ala4405Thr
|
|
ENST00000693060.1:c.13426G>A
|
ENSP00000510329.1:p.Ala4476Thr
|
|
ENST00000345136.8:c.13495G>A
MANE Select
|
ENSP00000344848.3:p.Ala4499Thr
|
|
ENST00000527303.2:c.10195G>A
|
ENSP00000433982.2:p.Ala3399Thr
|
|
ENST00000322810.8:c.13906G>A
|
ENSP00000323856.4:p.Ala4636Thr
|
|
ENST00000345136.7:c.13495G>A
|
ENSP00000344848.3:p.Ala4499Thr
|
|
ENST00000354589.7:c.13495G>A
|
ENSP00000346602.3:p.Ala4499Thr
|
|
ENST00000354958.6:c.13429G>A
|
ENSP00000347044.2:p.Ala4477Thr
|
|
ENST00000356346.7:c.13453G>A
MANE Plus Clinical
|
ENSP00000348702.3:p.Ala4485Thr
|
|
ENST00000357649.6:c.13507G>A
|
ENSP00000350277.2:p.Ala4503Thr
|
|
ENST00000398774.6:c.13399G>A
|
ENSP00000381756.2:p.Ala4467Thr
|
|
ENST00000436759.6:c.13576G>A
|
ENSP00000388180.2:p.Ala4526Thr
|
|
ENST00000527096.5:c.13564G>A
|
ENSP00000434583.1:p.Ala4522Thr
|
|
NM_000445.4:c.13576G>A
|
NP_000436.2:p.Ala4526Thr
|
|
NM_201378.3:c.13453G>A
|
NP_958780.1:p.Ala4485Thr
|
|
NM_201379.2:c.13429G>A
|
NP_958781.1:p.Ala4477Thr
|
|
NM_201380.3:c.13906G>A
|
NP_958782.1:p.Ala4636Thr
|
|
NM_201381.2:c.13399G>A
|
NP_958783.1:p.Ala4467Thr
|
|
NM_201382.3:c.13495G>A
|
NP_958784.1:p.Ala4499Thr
|
|
NM_201383.2:c.13507G>A
|
NP_958785.1:p.Ala4503Thr
|
|
NM_201384.2:c.13495G>A
|
NP_958786.1:p.Ala4499Thr
|
|
XM_005250976.2:c.13921G>A
|
XP_005251033.1:p.Ala4641Thr
|
|
XM_005250978.2:c.13522G>A
|
XP_005251035.1:p.Ala4508Thr
|
|
XM_005250979.3:c.13510G>A
|
XP_005251036.1:p.Ala4504Thr
|
|
XM_005250980.3:c.13510G>A
|
XP_005251037.1:p.Ala4504Thr
|
|
XM_005250981.2:c.13468G>A
|
XP_005251038.1:p.Ala4490Thr
|
|
XM_005250982.2:c.13444G>A
|
XP_005251039.1:p.Ala4482Thr
|
|
XM_005250983.2:c.13426G>A
|
XP_005251040.1:p.Ala4476Thr
|
|
XM_005250984.3:c.13414G>A
|
XP_005251041.1:p.Ala4472Thr
|
|
XM_006716588.2:c.13591G>A
|
XP_006716651.1:p.Ala4531Thr
|
|
XM_006716589.2:c.13441G>A
|
XP_006716652.1:p.Ala4481Thr
|
|
XM_006716590.2:c.13441G>A
|
XP_006716653.1:p.Ala4481Thr
|
|
XM_011517130.1:c.13510G>A
|
XP_011515432.1:p.Ala4504Thr
|
|
XM_011517131.1:c.13426G>A
|
XP_011515433.1:p.Ala4476Thr
|
|
XM_011517132.1:c.10141G>A
|
XP_011515434.1:p.Ala3381Thr
|
|
XM_005250976.4:c.13921G>A
|
XP_005251033.1:p.Ala4641Thr
|
|
XM_005250978.3:c.13522G>A
|
XP_005251035.1:p.Ala4508Thr
|
|
XM_005250979.4:c.13510G>A
|
XP_005251036.1:p.Ala4504Thr
|
|
XM_005250980.4:c.13510G>A
|
XP_005251037.1:p.Ala4504Thr
|
|
XM_005250981.3:c.13468G>A
|
XP_005251038.1:p.Ala4490Thr
|
|
XM_005250982.4:c.13444G>A
|
XP_005251039.1:p.Ala4482Thr
|
|
XM_005250984.5:c.13414G>A
|
XP_005251041.1:p.Ala4472Thr
|
|
XM_006716588.3:c.13591G>A
|
XP_006716651.1:p.Ala4531Thr
|
|
XM_006716590.3:c.13441G>A
|
XP_006716653.1:p.Ala4481Thr
|
|
XM_011517130.2:c.13510G>A
|
XP_011515432.1:p.Ala4504Thr
|
|
XM_011517131.2:c.13426G>A
|
XP_011515433.1:p.Ala4476Thr
|
|
XM_011517132.2:c.10141G>A
|
XP_011515434.1:p.Ala3381Thr
|
|
NM_000445.5:c.13576G>A
|
NP_000436.2:p.Ala4526Thr
|
|
NM_201378.4:c.13453G>A
MANE Plus Clinical
|
NP_958780.1:p.Ala4485Thr
|
|
NM_201379.3:c.13429G>A
|
NP_958781.1:p.Ala4477Thr
|
|
NM_201380.4:c.13906G>A
|
NP_958782.1:p.Ala4636Thr
|
|
NM_201381.3:c.13399G>A
|
NP_958783.1:p.Ala4467Thr
|
|
NM_201382.4:c.13495G>A
|
NP_958784.1:p.Ala4499Thr
|
|
NM_201383.3:c.13507G>A
|
NP_958785.1:p.Ala4503Thr
|
|
NM_201384.3:c.13495G>A
MANE Select
|
NP_958786.1:p.Ala4499Thr
|
|