ENST00000247933.9:c.1646G>A
|
ENSP00000247933.4:p.Gly549Glu
|
|
ENST00000514224.2:c.1646G>A
MANE Select
|
ENSP00000425081.2:p.Gly549Glu
|
|
ENST00000652070.1:n.1702G>A
|
|
|
ENST00000247933.8:c.1646G>A
|
ENSP00000247933.4:p.Gly549Glu
|
|
ENST00000514224.1:c.1250G>A
|
ENSP00000425081.1:p.Gly417Glu
|
|
ENST00000514417.1:n.38G>A
|
|
|
ENST00000514698.5:n.1753G>A
|
|
|
NM_000203.4:c.1646G>A
|
NP_000194.2:p.Gly549Glu
|
|
NR_110313.1:n.1734G>A
|
|
|
XM_006713882.2:c.1250G>A
|
XP_006713945.1:p.Gly417Glu
|
|
XM_011513459.1:c.1712G>A
|
XP_011511761.1:p.Gly571Glu
|
|
XM_011513460.1:c.1505G>A
|
XP_011511762.1:p.Gly502Glu
|
|
XM_011513461.1:c.1439G>A
|
XP_011511763.1:p.Gly480Glu
|
|
XM_011513462.1:c.1358G>A
|
XP_011511764.1:p.Gly453Glu
|
|
XM_011513463.1:c.1358G>A
|
XP_011511765.1:p.Gly453Glu
|
|
XR_924947.1:n.1902G>A
|
|
|
NM_000203.5:c.1646G>A
MANE Select
|
NP_000194.2:p.Gly549Glu
|
|
NM_001363576.1:c.1250G>A
|
NP_001350505.1:p.Gly417Glu
|
|
XM_011513461.2:c.1439G>A
|
XP_011511763.1:p.Gly480Glu
|
|
XM_017008163.1:c.686G>A
|
XP_016863652.1:p.Gly229Glu
|
|