ENST00000697337.1:c.*2585A>T
|
ENSP00000513259.1:n.*2585A>T
|
|
ENST00000697338.1:c.1697A>T
|
ENSP00000513260.1:n.1697A>T
|
|
ENST00000697339.1:c.883A>T
|
ENSP00000513261.1:p.Asn295Tyr
|
|
ENST00000697340.1:c.*566A>T
|
ENSP00000513262.1:n.*566A>T
|
|
ENST00000697341.1:n.1819A>T
|
|
|
ENST00000313735.11:c.1849A>T
MANE Select
|
ENSP00000327251.6:p.Asn617Tyr
|
|
ENST00000646938.1:c.1846A>T
|
ENSP00000494870.1:p.Asn616Tyr
|
|
ENST00000313735.10:c.1849A>T
|
ENSP00000327251.6:p.Asn617Tyr
|
|
ENST00000621962.1:c.1732A>T
|
ENSP00000482291.1:p.Asn578Tyr
|
|
NM_000625.4:c.1849A>T
MANE Select
|
NP_000616.3:p.Asn617Tyr
|
|
XM_011524859.1:c.1849A>T
|
XP_011523161.1:p.Asn617Tyr
|
|
XM_011524860.1:c.1846A>T
|
XP_011523162.1:p.Asn616Tyr
|
|
XM_011524861.1:c.1849A>T
|
XP_011523163.1:p.Asn617Tyr
|
|
XM_011524862.1:c.1183A>T
|
XP_011523164.1:p.Asn395Tyr
|
|