ENST00000360215.3:c.597G>C
MANE Select
|
ENSP00000353346.1:p.Leu199Phe
|
|
ENST00000496656.2:n.376G>C
|
|
|
ENST00000651132.1:c.597G>C
|
ENSP00000498322.1:p.Leu199Phe
|
|
ENST00000651676.1:c.597G>C
|
ENSP00000498699.1:p.Leu199Phe
|
|
ENST00000651994.1:c.*70-4707G>C
|
ENSP00000498310.1:n.*70-4707G>C
|
|
ENST00000652718.1:c.429G>C
|
ENSP00000498866.1:p.Leu143Phe
|
|
ENST00000360215.2:c.597G>C
|
ENSP00000353346.1:p.Leu199Phe
|
|
ENST00000496656.1:n.376G>C
|
|
|
NM_182548.3:c.597G>C
|
NP_872354.1:p.Leu199Phe
|
|
XM_011514403.1:c.597G>C
|
XP_011512705.1:p.Leu199Phe
|
|
NM_182548.4:c.597G>C
MANE Select
|
NP_872354.1:p.Leu199Phe
|
|