ENST00000330684.4:c.4147C>G
MANE Select
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ENSP00000332549.3:p.Pro1383Ala
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ENST00000535259.6:c.3333C>G
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ENSP00000441572.3:p.Ala1111=
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ENST00000636273.2:n.3397C>G
|
|
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ENST00000674742.1:c.3676C>G
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ENSP00000502200.1:p.Pro1226Ala
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ENST00000675398.1:c.*1517C>G
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ENSP00000502752.1:n.*1517C>G
|
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ENST00000330684.3:c.4147C>G
|
ENSP00000332549.3:p.Pro1383Ala
|
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ENST00000396573.6:c.4147C>G
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ENSP00000379818.2:p.Pro1383Ala
|
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ENST00000396575.6:c.3736C>G
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ENSP00000379820.3:p.Pro1246Ala
|
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ENST00000461292.3:n.3443C>G
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|
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ENST00000535259.5:c.3393C>G
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ENSP00000441572.2:p.Ala1131=
|
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ENST00000562109.5:c.3804C>G
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ENSP00000454998.1:p.Ala1268=
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NM_000833.4:c.4147C>G
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NP_000824.1:p.Pro1383Ala
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NM_001134407.2:c.4147C>G
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NP_001127879.1:p.Pro1383Ala
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NM_001134408.2:c.3804C>G
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NP_001127880.1:p.Ala1268=
|
|
XM_011522456.1:c.3988C>G
|
XP_011520758.1:p.Pro1330Ala
|
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XM_011522457.1:c.3889C>G
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XP_011520759.1:p.Pro1297Ala
|
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XM_011522458.1:c.3676C>G
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XP_011520760.1:p.Pro1226Ala
|
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XM_011522459.1:c.3676C>G
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XP_011520761.1:p.Pro1226Ala
|
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XM_011522460.1:c.3676C>G
|
XP_011520762.1:p.Pro1226Ala
|
|
XM_011522461.1:c.3804C>G
|
XP_011520763.1:p.Ala1268=
|
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XM_011522458.3:c.3676C>G
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XP_011520760.1:p.Pro1226Ala
|
|
XM_011522461.3:c.3804C>G
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XP_011520763.1:p.Ala1268=
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|
XM_017023172.1:c.4303C>G
|
XP_016878661.1:p.Pro1435Ala
|
|
XM_017023173.1:c.3960C>G
|
XP_016878662.1:p.Ala1320=
|
|
NM_001134407.3:c.4147C>G
MANE Select
|
NP_001127879.1:p.Pro1383Ala
|
|
NM_000833.5:c.4147C>G
|
NP_000824.1:p.Pro1383Ala
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