ENST00000295897.9:c.606G>C
MANE Select
|
ENSP00000295897.4:p.Leu202=
|
|
ENST00000295897.8:c.606G>C
|
ENSP00000295897.4:p.Leu202=
|
|
ENST00000401494.7:c.261G>C
|
ENSP00000384695.3:p.Leu87=
|
|
ENST00000415165.6:c.138-2518G>C
|
ENSP00000401820.2:n.138-2518G>C
|
|
ENST00000476441.6:c.203G>C
|
ENSP00000423727.1:p.Cys68Ser
|
|
ENST00000503124.5:c.156G>C
|
ENSP00000421027.1:p.Leu52=
|
|
ENST00000505649.5:n.292G>C
|
|
|
ENST00000509063.5:c.606G>C
|
ENSP00000422784.1:p.Leu202=
|
|
ENST00000511370.1:c.139G>C
|
|
|
ENST00000514786.1:n.575G>C
|
|
|
ENST00000621085.4:c.490+116G>C
|
ENSP00000483421.1:n.490+116G>C
|
|
ENST00000621628.4:c.486+402G>C
|
ENSP00000480485.1:n.486+402G>C
|
|
NM_000477.5:c.606G>C
|
NP_000468.1:p.Leu202=
|
|
NM_000477.6:c.606G>C
|
NP_000468.1:p.Leu202=
|
|
NM_000477.7:c.606G>C
MANE Select
|
NP_000468.1:p.Leu202=
|
|