ENST00000454220.7:c.670G>A
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ENSP00000391905.3:p.Ala224Thr
|
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ENST00000703395.1:c.13G>A
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ENSP00000515286.1:p.Ala5Thr
|
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ENST00000703396.1:n.494G>A
|
|
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ENST00000703397.1:c.13G>A
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ENSP00000515287.1:p.Ala5Thr
|
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ENST00000703398.1:c.592G>A
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ENSP00000515288.1:p.Ala198Thr
|
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ENST00000703421.1:n.703G>A
|
|
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ENST00000703422.1:c.526G>A
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ENSP00000515292.1:p.Ala176Thr
|
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ENST00000703423.1:c.13G>A
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ENSP00000515293.1:p.Ala5Thr
|
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ENST00000322088.11:c.550G>A
MANE Select
|
ENSP00000324804.6:p.Ala184Thr
|
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ENST00000322088.10:c.550G>A
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ENSP00000324804.6:p.Ala184Thr
|
|
ENST00000454220.6:c.670G>A
|
ENSP00000391905.2:p.Ala224Thr
|
|
ENST00000462047.1:n.241G>A
|
|
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ENST00000462990.5:c.13G>A
|
ENSP00000470504.1:p.Ala5Thr
|
|
NM_014225.5:c.550G>A
|
NP_055040.2:p.Ala184Thr
|
|
NR_033500.1:n.744G>A
|
|
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NM_001363656.1:c.13G>A
|
NP_001350585.1:p.Ala5Thr
|
|
NM_014225.6:c.550G>A
MANE Select
|
NP_055040.2:p.Ala184Thr
|
|
NM_001363656.2:c.13G>A
|
NP_001350585.1:p.Ala5Thr
|
|
NR_033500.2:n.494G>A
|
|
|