ENST00000396043.4:c.*328G>T
|
ENSP00000379358.4:n.*328G>T
|
|
ENST00000374690.9:c.1980G>T
MANE Select
|
ENSP00000363822.3:p.Leu660=
|
|
ENST00000396043.3:c.607G>T
|
ENSP00000379358.3:n.607G>T
|
|
ENST00000396044.8:c.1980G>T
|
ENSP00000379359.3:p.Leu660=
|
|
ENST00000612452.5:c.1980G>T
|
ENSP00000484033.2:p.Leu660=
|
|
ENST00000374690.7:c.1980G>T
|
ENSP00000363822.3:p.Leu660=
|
|
ENST00000396043.2:c.384G>T
|
ENSP00000379358.2:p.Leu128=
|
|
ENST00000396044.7:c.1980G>T
|
ENSP00000379359.3:p.Leu660=
|
|
ENST00000612452.4:c.1410G>T
|
ENSP00000484033.1:p.Leu470=
|
|
NM_000044.3:c.1980G>T
|
NP_000035.2:p.Leu660=
|
|
NM_001011645.2:c.384G>T
|
NP_001011645.1:p.Leu128=
|
|
NM_000044.4:c.1980G>T
|
NP_000035.2:p.Leu660=
|
|
NM_001011645.3:c.384G>T
|
NP_001011645.1:p.Leu128=
|
|
NM_000044.6:c.1980G>T
MANE Select
|
NP_000035.2:p.Leu660=
|
|