ENST00000295897.9:c.1514T>C
MANE Select
|
ENSP00000295897.4:p.Leu505Ser
|
|
ENST00000295897.8:c.1514T>C
|
ENSP00000295897.4:p.Leu505Ser
|
|
ENST00000401494.7:c.1169T>C
|
ENSP00000384695.3:p.Leu390Ser
|
|
ENST00000415165.6:c.938T>C
|
ENSP00000401820.2:p.Leu313Ser
|
|
ENST00000476441.6:c.*793T>C
|
ENSP00000423727.1:n.*793T>C
|
|
ENST00000486939.1:n.168T>C
|
|
|
ENST00000503124.5:c.1064T>C
|
ENSP00000421027.1:p.Leu355Ser
|
|
ENST00000505649.5:n.1061T>C
|
|
|
ENST00000509063.5:c.1514T>C
|
ENSP00000422784.1:p.Leu505Ser
|
|
ENST00000511370.1:c.1047T>C
|
|
|
ENST00000621085.4:c.875T>C
|
ENSP00000483421.1:p.Leu292Ser
|
|
ENST00000621628.4:c.875T>C
|
ENSP00000480485.1:p.Leu292Ser
|
|
NM_000477.5:c.1514T>C
|
NP_000468.1:p.Leu505Ser
|
|
NM_000477.6:c.1514T>C
|
NP_000468.1:p.Leu505Ser
|
|
NM_000477.7:c.1514T>C
MANE Select
|
NP_000468.1:p.Leu505Ser
|
|