ENST00000623535.2:c.2673G>T
MANE Select
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ENSP00000485244.1:p.Gln891His
|
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ENST00000674046.1:c.2796G>T
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ENSP00000501174.1:p.Gln932His
|
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ENST00000379989.6:c.2673G>T
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ENSP00000369325.3:p.Gln891His
|
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ENST00000379996.7:c.2673G>T
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ENSP00000369332.3:p.Gln891His
|
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ENST00000623535.1:c.2673G>T
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ENSP00000485244.1:p.Gln891His
|
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NM_001037343.1:c.2673G>T
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NP_001032420.1:p.Gln891His
|
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NM_003159.2:c.2673G>T
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NP_003150.1:p.Gln891His
|
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XM_011545569.1:c.2745G>T
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XP_011543871.1:p.Gln915His
|
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XM_011545570.1:c.2664G>T
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XP_011543872.1:p.Gln888His
|
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XR_950484.1:n.3048G>T
|
|
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NM_001323289.1:c.2673G>T
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NP_001310218.1:p.Gln891His
|
|
NM_001323289.2:c.2673G>T
MANE Select
|
NP_001310218.1:p.Gln891His
|
|
NM_001037343.2:c.2673G>T
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NP_001032420.1:p.Gln891His
|
|
NM_003159.3:c.2673G>T
|
NP_003150.1:p.Gln891His
|
|