ENST00000247933.9:c.1691T>A
|
ENSP00000247933.4:p.Leu564Gln
|
|
ENST00000514224.2:c.1691T>A
MANE Select
|
ENSP00000425081.2:p.Leu564Gln
|
|
ENST00000652070.1:n.1747T>A
|
|
|
ENST00000247933.8:c.1691T>A
|
ENSP00000247933.4:p.Leu564Gln
|
|
ENST00000514224.1:c.1295T>A
|
ENSP00000425081.1:p.Leu432Gln
|
|
ENST00000514417.1:n.83T>A
|
|
|
ENST00000514698.5:n.1798T>A
|
|
|
NM_000203.4:c.1691T>A
|
NP_000194.2:p.Leu564Gln
|
|
NR_110313.1:n.1779T>A
|
|
|
XM_006713882.2:c.1295T>A
|
XP_006713945.1:p.Leu432Gln
|
|
XM_011513459.1:c.1757T>A
|
XP_011511761.1:p.Leu586Gln
|
|
XM_011513460.1:c.1550T>A
|
XP_011511762.1:p.Leu517Gln
|
|
XM_011513461.1:c.1484T>A
|
XP_011511763.1:p.Leu495Gln
|
|
XM_011513462.1:c.1403T>A
|
XP_011511764.1:p.Leu468Gln
|
|
XM_011513463.1:c.1403T>A
|
XP_011511765.1:p.Leu468Gln
|
|
XR_924947.1:n.1947T>A
|
|
|
NM_000203.5:c.1691T>A
MANE Select
|
NP_000194.2:p.Leu564Gln
|
|
NM_001363576.1:c.1295T>A
|
NP_001350505.1:p.Leu432Gln
|
|
XM_011513461.2:c.1484T>A
|
XP_011511763.1:p.Leu495Gln
|
|
XM_017008163.1:c.731T>A
|
XP_016863652.1:p.Leu244Gln
|
|