ENST00000322048.12:c.414G=
MANE Select
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ENSP00000322832.6:p.Thr138=
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ENST00000322048.11:c.414G=
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ENSP00000322832.5:p.Thr138=
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|
ENST00000585653.1:n.546G=
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|
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ENST00000586153.1:c.159G=
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ENSP00000464699.1:p.Thr53=
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|
ENST00000586336.5:n.513G=
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|
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ENST00000586504.5:c.194G=
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|
|
ENST00000587377.5:c.414G=
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ENSP00000468343.1:p.Thr138=
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|
ENST00000587711.5:c.118-1037G=
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ENSP00000467459.1:n.118-1037G=
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|
ENST00000587843.5:c.*152G=
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ENSP00000465970.1:n.*152G=
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ENST00000588201.5:c.*271G=
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ENSP00000466529.1:n.*271G=
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ENST00000589543.5:n.371G=
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|
|
ENST00000591292.5:n.1743G=
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|
|
ENST00000591392.5:c.342G=
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ENSP00000467509.1:p.Thr114=
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|
ENST00000592019.1:c.76+57G=
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|
|
NM_024589.2:c.414G= , LRG_455t1:c.414G=
|
NP_078865.1:p.Thr138=
|
|
NR_046480.1:n.738G=
|
|
|
XM_006720947.2:c.414G=
|
XP_006721010.1:p.Thr138=
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XM_006720948.2:c.144G=
|
XP_006721011.1:p.Thr48=
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|
XM_006720947.4:c.414G=
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XP_006721010.1:p.Thr138=
|
|
XM_006720948.4:c.144G=
|
XP_006721011.1:p.Thr48=
|
|
NM_024589.3:c.414G=
MANE Select
|
NP_078865.1:p.Thr138=
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|
NR_046480.2:n.421G=
|
|
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