ENST00000413620.6:c.1115A>G
|
ENSP00000398579.2:p.Gln372Arg
|
|
ENST00000422680.6:c.1151A>G
|
ENSP00000390368.3:p.Gln384Arg
|
|
ENST00000440286.6:c.1151A>G
|
ENSP00000394934.2:p.Gln384Arg
|
|
ENST00000445622.6:c.1151A>G
|
ENSP00000395205.2:p.Gln384Arg
|
|
ENST00000615186.5:c.749A>G
|
ENSP00000479144.2:p.Gln250Arg
|
|
ENST00000689906.1:c.998A>G
|
ENSP00000508630.1:p.Gln333Arg
|
|
ENST00000692948.1:c.1208A>G
|
ENSP00000508773.1:p.Gln403Arg
|
|
ENST00000594239.6:c.1151A>G
MANE Select
|
ENSP00000471166.1:p.Gln384Arg
|
|
ENST00000594239.5:c.1151A>G
|
ENSP00000471166.1:p.Gln384Arg
|
|
ENST00000611071.4:c.1151A>G
|
ENSP00000479662.1:p.Gln384Arg
|
|
ENST00000611176.4:c.854A>G
|
ENSP00000478616.1:p.Gln285Arg
|
|
ENST00000612051.1:c.*1143A>G
|
ENSP00000480431.1:n.*1143A>G
|
|
ENST00000615874.4:c.1127A>G
|
ENSP00000483381.1:p.Gln376Arg
|
|
ENST00000617207.4:c.1148A>G
|
ENSP00000484023.1:p.Gln383Arg
|
|
ENST00000618670.4:c.1355A>G
|
ENSP00000483825.1:p.Gln452Arg
|
|
ENST00000619941.4:c.1130A>G
|
ENSP00000478979.1:p.Gln377Arg
|
|
NM_001099856.3:c.1355A>G
|
NP_001093326.2:p.Gln452Arg
|
|
NM_001099857.2:c.1151A>G
|
NP_001093327.1:p.Gln384Arg
|
|
NM_001145255.2:c.854A>G
|
NP_001138727.1:p.Gln285Arg
|
|
NM_003639.4:c.1151A>G
|
NP_003630.1:p.Gln384Arg
|
|
XM_005274760.3:c.1352A>G
|
XP_005274817.1:p.Gln451Arg
|
|
XM_005274761.3:c.1321+332A>G
|
XP_005274818.1:n.1321+332A>G
|
|
XM_005274764.3:c.1148A>G
|
XP_005274821.1:p.Gln383Arg
|
|
XM_011531203.1:c.1202A>G
|
XP_011529505.1:p.Gln401Arg
|
|
XM_011531204.1:c.1151A>G
|
XP_011529506.1:p.Gln384Arg
|
|
XM_011531205.1:c.1151A>G
|
XP_011529507.1:p.Gln384Arg
|
|
NM_001099856.4:c.1355A>G
|
NP_001093326.2:p.Gln452Arg
|
|
NM_001321396.1:c.1151A>G
|
NP_001308325.1:p.Gln384Arg
|
|
NM_001321397.1:c.1148A>G
|
NP_001308326.1:p.Gln383Arg
|
|
NM_001099856.6:c.1355A>G
|
NP_001093326.2:p.Gln452Arg
|
|
NM_001099857.4:c.1151A>G
|
NP_001093327.1:p.Gln384Arg
|
|
NM_001145255.4:c.854A>G
|
NP_001138727.1:p.Gln285Arg
|
|
NM_001321396.3:c.1151A>G
|
NP_001308325.1:p.Gln384Arg
|
|
NM_001321397.3:c.1148A>G
|
NP_001308326.1:p.Gln383Arg
|
|
NM_001377312.1:c.1151A>G
|
NP_001364241.1:p.Gln384Arg
|
|
NM_001377313.1:c.1148A>G
|
NP_001364242.1:p.Gln383Arg
|
|
NM_001377314.1:c.995A>G
|
NP_001364243.1:p.Gln332Arg
|
|
NM_001377315.1:c.782A>G
|
NP_001364244.1:p.Gln261Arg
|
|
NR_165197.1:n.1020A>G
|
|
|
NM_001099857.5:c.1151A>G
MANE Select
|
NP_001093327.1:p.Gln384Arg
|
|