ENST00000247933.9:c.1697T>C
|
ENSP00000247933.4:p.Leu566Pro
|
|
ENST00000514224.2:c.1697T>C
MANE Select
|
ENSP00000425081.2:p.Leu566Pro
|
|
ENST00000652070.1:n.1753T>C
|
|
|
ENST00000247933.8:c.1697T>C
|
ENSP00000247933.4:p.Leu566Pro
|
|
ENST00000514224.1:c.1301T>C
|
ENSP00000425081.1:p.Leu434Pro
|
|
ENST00000514417.1:n.89T>C
|
|
|
ENST00000514698.5:n.1804T>C
|
|
|
NM_000203.4:c.1697T>C
|
NP_000194.2:p.Leu566Pro
|
|
NR_110313.1:n.1785T>C
|
|
|
XM_006713882.2:c.1301T>C
|
XP_006713945.1:p.Leu434Pro
|
|
XM_011513459.1:c.1763T>C
|
XP_011511761.1:p.Leu588Pro
|
|
XM_011513460.1:c.1556T>C
|
XP_011511762.1:p.Leu519Pro
|
|
XM_011513461.1:c.1490T>C
|
XP_011511763.1:p.Leu497Pro
|
|
XM_011513462.1:c.1409T>C
|
XP_011511764.1:p.Leu470Pro
|
|
XM_011513463.1:c.1409T>C
|
XP_011511765.1:p.Leu470Pro
|
|
XR_924947.1:n.1953T>C
|
|
|
NM_000203.5:c.1697T>C
MANE Select
|
NP_000194.2:p.Leu566Pro
|
|
NM_001363576.1:c.1301T>C
|
NP_001350505.1:p.Leu434Pro
|
|
XM_011513461.2:c.1490T>C
|
XP_011511763.1:p.Leu497Pro
|
|
XM_017008163.1:c.737T>C
|
XP_016863652.1:p.Leu246Pro
|
|