ENST00000301305.8:c.1234G>A
MANE Select
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ENSP00000301305.4:p.Ala412Thr
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ENST00000276833.9:c.1159G>A
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ENSP00000276833.5:p.Ala387Thr
|
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ENST00000301305.7:c.1234G>A
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ENSP00000301305.3:p.Ala412Thr
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ENST00000531789.1:n.71G>A
|
|
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NM_017767.2:c.1159G>A
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NP_060237.2:p.Ala387Thr
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NM_130849.3:c.1234G>A
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NP_570901.2:p.Ala412Thr
|
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XM_006716599.1:c.1234G>A
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XP_006716662.1:p.Ala412Thr
|
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XM_011517153.1:c.952G>A
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XP_011515455.1:p.Ala318Thr
|
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XM_024447188.1:c.952G>A
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XP_024302956.1:p.Ala318Thr
|
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XM_024447189.1:c.952G>A
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XP_024302957.1:p.Ala318Thr
|
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NM_001374839.1:c.952G>A
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NP_001361768.1:p.Ala318Thr
|
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NM_017767.3:c.1159G>A
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NP_060237.3:p.Ala387Thr
|
|
NM_130849.4:c.1234G>A
MANE Select
|
NP_570901.3:p.Ala412Thr
|
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