ENST00000409052.6:c.266T>C
|
ENSP00000387210.1:p.Phe89Ser
|
|
ENST00000696879.1:c.266T>C
|
ENSP00000512947.1:p.Phe89Ser
|
|
ENST00000696880.1:c.266T>C
|
ENSP00000512948.1:p.Phe89Ser
|
|
ENST00000696881.1:c.266T>C
|
ENSP00000512949.1:p.Phe89Ser
|
|
ENST00000696882.1:c.*138T>C
|
ENSP00000512950.1:n.*138T>C
|
|
ENST00000696883.1:n.313T>C
|
|
|
ENST00000409930.4:c.368T>C
MANE Select
|
ENSP00000387173.3:p.Phe123Ser
|
|
ENST00000259206.9:c.377T>C
|
ENSP00000259206.5:p.Phe126Ser
|
|
ENST00000354115.6:c.314T>C
|
ENSP00000329072.3:p.Phe105Ser
|
|
ENST00000361779.7:c.266T>C
|
ENSP00000354816.3:p.Phe89Ser
|
|
ENST00000409052.5:c.266T>C
|
ENSP00000387210.1:p.Phe89Ser
|
|
ENST00000409930.3:c.368T>C
|
ENSP00000387173.3:p.Phe123Ser
|
|
NM_000577.4:c.314T>C
|
NP_000568.1:p.Phe105Ser
|
|
NM_173841.2:c.377T>C , LRG_188t1:c.377T>C
|
NP_776213.1:p.Phe126Ser
|
|
NM_173842.2:c.368T>C
|
NP_776214.1:p.Phe123Ser
|
|
NM_173843.2:c.266T>C
|
NP_776215.1:p.Phe89Ser
|
|
XM_005263661.3:c.266T>C
|
XP_005263718.1:p.Phe89Ser
|
|
XM_006712497.2:c.266T>C
|
XP_006712560.1:p.Phe89Ser
|
|
XM_011511121.1:c.266T>C
|
XP_011509423.1:p.Phe89Ser
|
|
NM_001318914.1:c.266T>C
|
NP_001305843.1:p.Phe89Ser
|
|
XM_005263661.4:c.266T>C
|
XP_005263718.1:p.Phe89Ser
|
|
NM_000577.5:c.314T>C
|
NP_000568.1:p.Phe105Ser
|
|
NM_001318914.2:c.266T>C
|
NP_001305843.1:p.Phe89Ser
|
|
NM_173842.3:c.368T>C
MANE Select
|
NP_776214.1:p.Phe123Ser
|
|
NM_173843.3:c.266T>C
|
NP_776215.1:p.Phe89Ser
|
|
NM_001379360.1:c.266T>C
|
NP_001366289.1:p.Phe89Ser
|
|
NM_173841.3:c.377T>C
|
NP_776213.1:p.Phe126Ser
|
|