ENST00000395958.6:c.699A>C
MANE Select
|
ENSP00000379288.2:p.Gln233His
|
|
ENST00000353245.7:c.699A>C
|
ENSP00000309503.3:p.Gln233His
|
|
ENST00000395948.6:c.468A>C
|
ENSP00000379278.2:p.Gln156His
|
|
ENST00000395951.7:c.699A>C
|
ENSP00000379281.3:p.Gln233His
|
|
ENST00000395953.6:c.699A>C
|
ENSP00000379283.2:p.Gln233His
|
|
ENST00000395956.7:c.699A>C
|
ENSP00000379286.3:p.Gln233His
|
|
ENST00000395957.6:c.699A>C
|
ENSP00000379287.2:p.Gln233His
|
|
ENST00000395958.5:c.699A>C
|
ENSP00000379288.2:p.Gln233His
|
|
ENST00000419477.6:c.699A>C
|
ENSP00000395114.2:p.Gln233His
|
|
ENST00000457309.2:c.699A>C
|
ENSP00000398599.1:p.Gln233His
|
|
ENST00000521309.5:c.339A>C
|
ENSP00000429623.1:p.Gln113His
|
|
ENST00000521607.5:c.723A>C
|
ENSP00000430058.1:p.Gln241His
|
|
ENST00000522542.5:c.474A>C
|
ENSP00000430072.1:p.Gln158His
|
|
ENST00000522819.5:c.339A>C
|
ENSP00000428775.1:p.Gln113His
|
|
ENST00000523848.5:c.354A>C
|
ENSP00000428860.1:p.Gln118His
|
|
NM_001135699.1:c.699A>C
|
NP_001129171.1:p.Gln233His
|
|
NM_001135700.1:c.699A>C
|
NP_001129172.1:p.Gln233His
|
|
NM_001135701.1:c.699A>C
|
NP_001129173.1:p.Gln233His
|
|
NM_001135702.1:c.699A>C
|
NP_001129174.1:p.Gln233His
|
|
NM_003406.3:c.699A>C
|
NP_003397.1:p.Gln233His
|
|
NM_145690.2:c.699A>C
|
NP_663723.1:p.Gln233His
|
|
XM_005251061.2:c.699A>C
|
XP_005251118.1:p.Gln233His
|
|
XM_005251062.2:c.699A>C
|
XP_005251119.1:p.Gln233His
|
|
XM_005251063.2:c.699A>C
|
XP_005251120.1:p.Gln233His
|
|
XM_011517289.1:c.699A>C
|
XP_011515591.1:p.Gln233His
|
|
XM_005251061.3:c.699A>C
|
XP_005251118.1:p.Gln233His
|
|
XM_005251063.3:c.699A>C
|
XP_005251120.1:p.Gln233His
|
|
XM_017013810.2:c.699A>C
|
XP_016869299.1:p.Gln233His
|
|
XM_017013811.1:c.699A>C
|
XP_016869300.1:p.Gln233His
|
|
XM_024447266.1:c.699A>C
|
XP_024303034.1:p.Gln233His
|
|
NM_145690.3:c.699A>C
MANE Select
|
NP_663723.1:p.Gln233His
|
|
NM_001135700.2:c.699A>C
|
NP_001129172.1:p.Gln233His
|
|
NM_001135701.2:c.699A>C
|
NP_001129173.1:p.Gln233His
|
|
NM_001135702.2:c.699A>C
|
NP_001129174.1:p.Gln233His
|
|
NM_003406.4:c.699A>C
|
NP_003397.1:p.Gln233His
|
|
NM_001135699.2:c.699A>C
|
NP_001129171.1:p.Gln233His
|
|