ENST00000247933.9:c.995T>A
|
ENSP00000247933.4:p.Leu332Gln
|
|
ENST00000514224.2:c.995T>A
MANE Select
|
ENSP00000425081.2:p.Leu332Gln
|
|
ENST00000652070.1:n.1051T>A
|
|
|
ENST00000247933.8:c.995T>A
|
ENSP00000247933.4:p.Leu332Gln
|
|
ENST00000514224.1:c.599T>A
|
ENSP00000425081.1:p.Leu200Gln
|
|
ENST00000514698.5:n.1102T>A
|
|
|
NM_000203.4:c.995T>A
|
NP_000194.2:p.Leu332Gln
|
|
NR_110313.1:n.1083T>A
|
|
|
XM_006713882.2:c.599T>A
|
XP_006713945.1:p.Leu200Gln
|
|
XM_011513459.1:c.1061T>A
|
XP_011511761.1:p.Leu354Gln
|
|
XM_011513460.1:c.854T>A
|
XP_011511762.1:p.Leu285Gln
|
|
XM_011513461.1:c.788T>A
|
XP_011511763.1:p.Leu263Gln
|
|
XM_011513462.1:c.707T>A
|
XP_011511764.1:p.Leu236Gln
|
|
XM_011513463.1:c.707T>A
|
XP_011511765.1:p.Leu236Gln
|
|
XR_924947.1:n.1064T>A
|
|
|
NM_000203.5:c.995T>A
MANE Select
|
NP_000194.2:p.Leu332Gln
|
|
NM_001363576.1:c.599T>A
|
NP_001350505.1:p.Leu200Gln
|
|
XM_011513461.2:c.788T>A
|
XP_011511763.1:p.Leu263Gln
|
|
XM_017008163.1:c.35T>A
|
XP_016863652.1:p.Leu12Gln
|
|