ENST00000371375.2:c.4519A>C
|
ENSP00000360426.1:p.Asn1507His
|
|
ENST00000685253.1:c.*1986A>C
|
ENSP00000509405.1:n.*1986A>C
|
|
ENST00000685889.1:n.2178A>C
|
|
|
ENST00000686807.1:n.862A>C
|
|
|
ENST00000686954.1:c.*727A>C
|
ENSP00000508416.1:n.*727A>C
|
|
ENST00000688810.1:c.4471A>C
|
ENSP00000509140.1:p.Asn1491His
|
|
ENST00000689233.1:n.9651A>C
|
|
|
ENST00000690340.1:n.3116A>C
|
|
|
ENST00000692286.1:c.5311A>C
|
ENSP00000509490.1:p.Asn1771His
|
|
ENST00000692396.1:c.5395A>C
|
ENSP00000508605.1:p.Asn1799His
|
|
ENST00000371380.8:c.5443A>C
MANE Select
|
ENSP00000360431.2:p.Asn1815His
|
|
ENST00000371385.8:c.4417A>C
|
ENSP00000360438.4:p.Asn1473His
|
|
ENST00000674738.1:c.3998A>C
|
|
|
ENST00000674827.1:c.3559A>C
|
ENSP00000502523.1:p.Asn1187His
|
|
ENST00000675218.1:c.4519A>C
|
ENSP00000501910.1:p.Asn1507His
|
|
ENST00000675487.1:c.*1376A>C
|
ENSP00000502340.1:n.*1376A>C
|
|
ENST00000675718.1:c.4712A>C
|
|
|
ENST00000260766.7:c.5443A>C
|
ENSP00000260766.3:p.Asn1815His
|
|
ENST00000371375.1:c.4519A>C
|
ENSP00000360426.1:p.Asn1507His
|
|
ENST00000371380.7:c.5443A>C
|
ENSP00000360431.2:p.Asn1815His
|
|
ENST00000371385.7:c.4519A>C
|
ENSP00000360438.3:p.Asn1507His
|
|
NM_001165979.2:c.4519A>C
|
NP_001159451.1:p.Asn1507His
|
|
NM_001288989.1:c.5395A>C
|
NP_001275918.1:p.Asn1799His
|
|
NM_016341.3:c.5443A>C
|
NP_057425.3:p.Asn1815His
|
|
XM_006717885.2:c.5485A>C
|
XP_006717948.1:p.Asn1829His
|
|
XM_006717886.2:c.5485A>C
|
XP_006717949.1:p.Asn1829His
|
|
XM_006717888.2:c.5482A>C
|
XP_006717951.1:p.Asn1828His
|
|
XM_006717889.2:c.5437A>C
|
XP_006717952.1:p.Asn1813His
|
|
XM_006717890.1:c.4561A>C
|
XP_006717953.1:p.Asn1521His
|
|
XM_011539849.1:c.5485A>C
|
XP_011538151.1:p.Asn1829His
|
|
XM_011539850.1:c.4330A>C
|
XP_011538152.1:p.Asn1444His
|
|
XM_006717885.4:c.5485A>C
|
XP_006717948.1:p.Asn1829His
|
|
XM_006717888.4:c.5482A>C
|
XP_006717951.1:p.Asn1828His
|
|
XM_006717889.4:c.5437A>C
|
XP_006717952.1:p.Asn1813His
|
|
XM_006717890.3:c.4561A>C
|
XP_006717953.1:p.Asn1521His
|
|
XM_011539849.3:c.5485A>C
|
XP_011538151.1:p.Asn1829His
|
|
XM_011539850.3:c.4330A>C
|
XP_011538152.1:p.Asn1444His
|
|
XM_017016310.2:c.5485A>C
|
XP_016871799.1:p.Asn1829His
|
|
XM_017016311.2:c.5485A>C
|
XP_016871800.1:p.Asn1829His
|
|
XM_017016312.2:c.4471A>C
|
XP_016871801.1:p.Asn1491His
|
|
NM_001288989.2:c.5395A>C
|
NP_001275918.1:p.Asn1799His
|
|
NM_016341.4:c.5443A>C
MANE Select
|
NP_057425.3:p.Asn1815His
|
|