ENST00000542664.4:c.513G>C
MANE Select
|
ENSP00000437737.1:p.Leu171=
|
|
ENST00000543956.5:c.24G>C
|
ENSP00000441861.2:p.Leu8=
|
|
ENST00000378688.8:c.513G>C
|
ENSP00000367959.3:p.Leu171=
|
|
ENST00000542664.3:c.513G>C
|
ENSP00000437737.1:p.Leu171=
|
|
ENST00000543956.4:c.261G>C
|
ENSP00000441861.1:p.Leu87=
|
|
NM_000621.4:c.513G>C
|
NP_000612.1:p.Leu171=
|
|
NM_001165947.2:c.261G>C
|
NP_001159419.1:p.Leu87=
|
|
NM_000621.5:c.513G>C
MANE Select
|
NP_000612.1:p.Leu171=
|
|
NM_001165947.5:c.24G>C
|
NP_001159419.2:p.Leu8=
|
|
NM_001378924.1:c.513G>C
|
NP_001365853.1:p.Leu171=
|
|