ENST00000247933.9:c.1553T>A
|
ENSP00000247933.4:p.Leu518Ter
|
|
ENST00000514224.2:c.1553T>A
MANE Select
|
ENSP00000425081.2:p.Leu518Ter
|
|
ENST00000652070.1:n.1609T>A
|
|
|
ENST00000247933.8:c.1553T>A
|
ENSP00000247933.4:p.Leu518Ter
|
|
ENST00000502829.1:n.542T>A
|
|
|
ENST00000514224.1:c.1157T>A
|
ENSP00000425081.1:p.Leu386Ter
|
|
ENST00000514698.5:n.1660T>A
|
|
|
NM_000203.4:c.1553T>A
|
NP_000194.2:p.Leu518Ter
|
|
NR_110313.1:n.1641T>A
|
|
|
XM_006713882.2:c.1157T>A
|
XP_006713945.1:p.Leu386Ter
|
|
XM_011513459.1:c.1619T>A
|
XP_011511761.1:p.Leu540Ter
|
|
XM_011513460.1:c.1412T>A
|
XP_011511762.1:p.Leu471Ter
|
|
XM_011513461.1:c.1346T>A
|
XP_011511763.1:p.Leu449Ter
|
|
XM_011513462.1:c.1265T>A
|
XP_011511764.1:p.Leu422Ter
|
|
XM_011513463.1:c.1265T>A
|
XP_011511765.1:p.Leu422Ter
|
|
XR_924947.1:n.1809T>A
|
|
|
NM_000203.5:c.1553T>A
MANE Select
|
NP_000194.2:p.Leu518Ter
|
|
NM_001363576.1:c.1157T>A
|
NP_001350505.1:p.Leu386Ter
|
|
XM_011513461.2:c.1346T>A
|
XP_011511763.1:p.Leu449Ter
|
|
XM_017008163.1:c.593T>A
|
XP_016863652.1:p.Leu198Ter
|
|