ENST00000396043.4:c.*991G>T
|
ENSP00000379358.4:n.*991G>T
|
|
ENST00000374690.9:c.2643G>T
MANE Select
|
ENSP00000363822.3:p.Leu881=
|
|
ENST00000396043.3:c.1270G>T
|
ENSP00000379358.3:n.1270G>T
|
|
ENST00000396044.8:c.*4G>T
|
ENSP00000379359.3:n.*4G>T
|
|
ENST00000612452.5:c.2643G>T
|
ENSP00000484033.2:p.Leu881=
|
|
ENST00000374690.7:c.2643G>T
|
ENSP00000363822.3:p.Leu881=
|
|
ENST00000396043.2:c.1047G>T
|
ENSP00000379358.2:p.Leu349=
|
|
ENST00000396044.7:c.*4G>T
|
ENSP00000379359.3:n.*4G>T
|
|
ENST00000612452.4:c.2094G>T
|
ENSP00000484033.1:p.Leu698=
|
|
NM_000044.3:c.2643G>T
|
NP_000035.2:p.Leu881=
|
|
NM_001011645.2:c.1047G>T
|
NP_001011645.1:p.Leu349=
|
|
NM_000044.4:c.2643G>T
|
NP_000035.2:p.Leu881=
|
|
NM_001011645.3:c.1047G>T
|
NP_001011645.1:p.Leu349=
|
|
NM_000044.6:c.2643G>T
MANE Select
|
NP_000035.2:p.Leu881=
|
|