ENST00000496887.7:c.779G>C
|
ENSP00000434560.2:p.Trp260Ser
|
|
ENST00000646564.2:c.596G>C
|
ENSP00000495806.2:p.Trp199Ser
|
|
ENST00000155840.12:c.1136G>C
MANE Select
|
ENSP00000155840.2:p.Trp379Ser
|
|
ENST00000335475.6:c.755G>C
|
ENSP00000334497.5:p.Trp252Ser
|
|
ENST00000646564.1:c.242G>C
|
ENSP00000495806.1:p.Trp81Ser
|
|
ENST00000155840.9:c.1136G>C
|
ENSP00000155840.2:p.Trp379Ser
|
|
ENST00000335475.5:c.755G>C
|
ENSP00000334497.5:p.Trp252Ser
|
|
NM_000218.2:c.1136G>C , LRG_287t1:c.1136G>C
|
NP_000209.2:p.Trp379Ser
|
|
NM_181798.1:c.755G>C , LRG_287t2:c.755G>C
|
NP_861463.1:p.Trp252Ser
|
|
NM_000218.3:c.1136G>C
MANE Select
|
NP_000209.2:p.Trp379Ser
|
|