ENST00000269321.12:c.592A>G
MANE Select
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ENSP00000269321.7:p.Ile198Val
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ENST00000269321.11:c.592A>G
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ENSP00000269321.7:p.Ile198Val
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ENST00000400721.8:c.460A>G
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ENSP00000383556.4:p.Ile154Val
|
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ENST00000541078.6:c.592A>G
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ENSP00000441348.2:p.Ile198Val
|
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ENST00000579121.5:c.502+90A>G
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ENSP00000462960.1:n.502+90A>G
|
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ENST00000580685.5:c.592A>G
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ENSP00000464205.1:p.Ile198Val
|
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ENST00000581876.5:c.367A>G
|
ENSP00000461956.1:p.Ile123Val
|
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ENST00000582984.5:n.794A>G
|
|
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ENST00000583868.5:c.480A>G
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ENSP00000462209.1:p.Pro160=
|
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ENST00000584461.5:c.502+90A>G
|
ENSP00000463939.1:n.502+90A>G
|
|
NM_001185077.2:c.592A>G
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NP_001172006.1:p.Ile198Val
|
|
NM_001185078.2:c.460A>G
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NP_001172007.1:p.Ile154Val
|
|
NM_001301240.1:c.502+90A>G
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NP_001288169.1:n.502+90A>G
|
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NM_001301241.1:c.502+90A>G
|
NP_001288170.1:n.502+90A>G
|
|
NM_001301242.1:c.480A>G
|
NP_001288171.1:p.Pro160=
|
|
NM_001301243.1:c.727A>G
|
NP_001288172.1:p.Ile243Val
|
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NM_004309.5:c.592A>G
|
NP_004300.1:p.Ile198Val
|
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NR_125441.1:n.651A>G
|
|
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XM_011523574.1:c.727A>G
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XP_011521876.1:p.Ile243Val
|
|
NM_004309.6:c.592A>G
MANE Select
|
NP_004300.1:p.Ile198Val
|
|
NM_001185077.3:c.592A>G
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NP_001172006.1:p.Ile198Val
|
|
NM_001185078.3:c.460A>G
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NP_001172007.1:p.Ile154Val
|
|
NM_001301240.2:c.502+90A>G
|
NP_001288169.1:n.502+90A>G
|
|
NM_001301241.2:c.502+90A>G
|
NP_001288170.1:n.502+90A>G
|
|
NM_001301242.2:c.480A>G
|
NP_001288171.1:p.Pro160=
|
|
NM_001301243.2:c.727A>G
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NP_001288172.1:p.Ile243Val
|
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NR_125441.2:n.582A>G
|
|
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