|
NM_018026.4:c.1098G>C
MANE Select
|
NP_060496.2:p.Leu366Phe
|
|
ENST00000320580.9:c.1098G>C
MANE Select
|
ENSP00000316454.4:p.Leu366Phe
|
|
NM_018026.3:c.1098G>C
|
NP_060496.2:p.Leu366Phe
|
|
ENST00000320580.8:c.1098G>C
|
ENSP00000316454.4:p.Leu366Phe
|
|
ENST00000524784.1:c.382G>C
|
ENSP00000435037.1:n.382G>C
|
|
ENST00000533811.1:n.403G>C
|
|
|
ENST00000534273.1:n.21G>C
|
|
|
XM_011545162.1:c.777G>C
|
XP_011543464.1:p.Leu259Phe
|
|
XM_011545163.1:c.768G>C
|
XP_011543465.1:p.Leu256Phe
|
|
XM_011545164.1:c.759G>C
|
XP_011543466.1:p.Leu253Phe
|
|
XM_011545164.2:c.759G>C
|
XP_011543466.1:p.Leu253Phe
|
|
XR_001747924.1:n.1309G>C
|
|