ENST00000356392.9:c.1227G>T
MANE Select
|
ENSP00000348757.3:p.Leu409=
|
|
ENST00000356392.8:c.1227G>T
|
ENSP00000348757.3:p.Leu409=
|
|
ENST00000586836.5:c.654G>T
|
ENSP00000467429.1:p.Leu218=
|
|
ENST00000591179.5:c.1047G>T
|
ENSP00000466800.1:p.Leu349=
|
|
ENST00000591345.5:c.*1146G>T
|
ENSP00000467313.1:n.*1146G>T
|
|
NM_001302453.1:c.1065G>T
|
NP_001289382.1:p.Leu355=
|
|
NM_001302454.1:c.1047G>T
|
NP_001289383.1:p.Leu349=
|
|
NM_145045.4:c.1227G>T
|
NP_659482.3:p.Leu409=
|
|
NM_145045.5:c.1227G>T
MANE Select
|
NP_659482.3:p.Leu409=
|
|
NM_001302454.2:c.1047G>T
|
NP_001289383.1:p.Leu349=
|
|