ENST00000317447.9:c.590C>A
|
ENSP00000320646.4:p.Ala197Asp
|
|
ENST00000614302.5:c.590C>A
MANE Select
|
ENSP00000479130.1:p.Ala197Asp
|
|
ENST00000649953.1:c.590C>A
|
ENSP00000497456.1:p.Ala197Asp
|
|
ENST00000317447.8:c.590C>A
|
ENSP00000320646.4:p.Ala197Asp
|
|
ENST00000378345.8:c.-129-1333C>A
|
ENSP00000367596.4:n.-129-1333C>A
|
|
ENST00000406948.7:c.590C>A
|
ENSP00000384627.3:p.Ala197Asp
|
|
ENST00000537290.5:c.590C>A
|
ENSP00000440734.1:p.Ala197Asp
|
|
ENST00000537895.5:c.-129-1333C>A
|
ENSP00000439201.1:n.-129-1333C>A
|
|
ENST00000540697.5:c.-129-1333C>A
|
ENSP00000445397.1:n.-129-1333C>A
|
|
ENST00000542688.5:c.590C>A
|
ENSP00000446281.1:p.Ala197Asp
|
|
ENST00000614302.4:c.590C>A
|
ENSP00000479130.1:p.Ala197Asp
|
|
NM_001127214.3:c.590C>A
|
NP_001120686.1:p.Ala197Asp
|
|
NM_001243279.2:c.590C>A
|
NP_001230208.1:p.Ala197Asp
|
|
NM_001284316.1:c.-129-1333C>A
|
NP_001271245.1:n.-129-1333C>A
|
|
NM_174917.4:c.590C>A
|
NP_777577.2:p.Ala197Asp
|
|
NR_104293.1:n.971C>A
|
|
|
XM_005256293.1:c.590C>A
|
XP_005256350.1:p.Ala197Asp
|
|
XM_011522942.1:c.590C>A
|
XP_011521244.1:p.Ala197Asp
|
|
XM_011522943.1:c.590C>A
|
XP_011521245.1:p.Ala197Asp
|
|
XM_011522944.1:c.590C>A
|
XP_011521246.1:p.Ala197Asp
|
|
XR_933238.1:n.934C>A
|
|
|
XR_933239.1:n.934C>A
|
|
|
XR_933240.1:n.934C>A
|
|
|
XR_933241.1:n.934C>A
|
|
|
NR_147928.1:n.971C>A
|
|
|
NR_147929.1:n.971C>A
|
|
|
XM_005256293.2:c.590C>A
|
XP_005256350.1:p.Ala197Asp
|
|
XM_017023018.1:c.590C>A
|
XP_016878507.1:p.Ala197Asp
|
|
XM_017023019.1:c.590C>A
|
XP_016878508.1:p.Ala197Asp
|
|
XM_017023020.2:c.-4419C>A
|
XP_016878509.1:n.-4419C>A
|
|
XM_017023021.1:c.590C>A
|
XP_016878510.1:p.Ala197Asp
|
|
XM_024450186.1:c.-129-1333C>A
|
XP_024305954.1:n.-129-1333C>A
|
|
XM_024450187.1:c.-129-1333C>A
|
XP_024305955.1:n.-129-1333C>A
|
|
XR_001751864.2:n.933C>A
|
|
|
XR_001751865.1:n.933C>A
|
|
|
XR_933238.2:n.933C>A
|
|
|
XR_933240.3:n.933C>A
|
|
|
NM_001127214.4:c.590C>A
|
NP_001120686.1:p.Ala197Asp
|
|
NM_001243279.3:c.590C>A
MANE Select
|
NP_001230208.1:p.Ala197Asp
|
|
NM_001284316.2:c.-129-1333C>A
|
NP_001271245.1:n.-129-1333C>A
|
|
NM_174917.5:c.590C>A
|
NP_777577.2:p.Ala197Asp
|
|
NR_104293.2:n.928C>A
|
|
|
NR_147928.2:n.928C>A
|
|
|
NR_147929.2:n.928C>A
|
|
|