ENST00000295897.9:c.1189G>T
MANE Select
|
ENSP00000295897.4:p.Val397Leu
|
|
ENST00000295897.8:c.1189G>T
|
ENSP00000295897.4:p.Val397Leu
|
|
ENST00000401494.7:c.844G>T
|
ENSP00000384695.3:p.Val282Leu
|
|
ENST00000415165.6:c.613G>T
|
ENSP00000401820.2:p.Val205Leu
|
|
ENST00000476441.6:c.*468G>T
|
ENSP00000423727.1:n.*468G>T
|
|
ENST00000484992.1:n.509G>T
|
|
|
ENST00000503124.5:c.739G>T
|
ENSP00000421027.1:p.Val247Leu
|
|
ENST00000504043.1:n.192G>T
|
|
|
ENST00000505649.5:n.875G>T
|
|
|
ENST00000509063.5:c.1189G>T
|
ENSP00000422784.1:p.Val397Leu
|
|
ENST00000511370.1:c.722G>T
|
|
|
ENST00000621085.4:c.550G>T
|
ENSP00000483421.1:p.Val184Leu
|
|
ENST00000621628.4:c.550G>T
|
ENSP00000480485.1:p.Val184Leu
|
|
NM_000477.5:c.1189G>T
|
NP_000468.1:p.Val397Leu
|
|
NM_000477.6:c.1189G>T
|
NP_000468.1:p.Val397Leu
|
|
NM_000477.7:c.1189G>T
MANE Select
|
NP_000468.1:p.Val397Leu
|
|