ENST00000370263.9:c.1715A=
MANE Select
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ENSP00000359285.4:p.Gln572=
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ENST00000370263.8:c.1715A=
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ENSP00000359285.4:p.Gln572=
|
|
ENST00000463705.5:n.2363A=
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|
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ENST00000467563.3:n.1785A=
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|
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ENST00000498043.6:c.1739A=
|
|
|
ENST00000615287.4:c.1502A=
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ENSP00000483388.1:p.Gln501=
|
|
ENST00000627000.1:c.*1404A=
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ENSP00000486914.1:n.*1404A=
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|
ENST00000630240.1:n.1436A=
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|
|
NM_000744.6:c.1715A=
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NP_000735.1:p.Gln572=
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|
NM_001256573.1:c.1187A=
|
NP_001243502.1:p.Gln396=
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|
NR_046317.1:n.1971A=
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|
|
XM_011528524.1:c.1502A=
|
XP_011526826.1:p.Gln501=
|
|
XM_017027625.2:c.1187A=
|
XP_016883114.1:p.Gln396=
|
|
XM_024451822.1:c.1187A=
|
XP_024307590.1:p.Gln396=
|
|
NM_001256573.2:c.1187A=
|
NP_001243502.1:p.Gln396=
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|
NR_046317.2:n.1924A=
|
|
|
NM_000744.7:c.1715A=
MANE Select
|
NP_000735.1:p.Gln572=
|
|