ENST00000233575.7:c.776T>C
MANE Select
|
ENSP00000233575.2:p.Phe259Ser
|
|
ENST00000233575.6:c.776T>C
|
ENSP00000233575.2:p.Phe259Ser
|
|
ENST00000427123.5:c.*586T>C
|
ENSP00000405399.1:n.*586T>C
|
|
ENST00000440760.5:c.*621T>C
|
ENSP00000399727.1:n.*621T>C
|
|
ENST00000453453.1:c.*303T>C
|
ENSP00000401922.1:n.*303T>C
|
|
ENST00000493711.1:n.493T>C
|
|
|
ENST00000494893.5:n.952T>C
|
|
|
ENST00000537606.5:c.701T>C
|
ENSP00000439208.1:p.Phe234Ser
|
|
NM_001267059.1:c.740T>C
|
NP_001253988.1:p.Phe247Ser
|
|
NM_001267060.1:c.701T>C
|
NP_001253989.1:p.Phe234Ser
|
|
NM_001267061.1:c.716T>C
|
NP_001253990.1:p.Phe239Ser
|
|
NM_014748.3:c.776T>C
|
NP_055563.1:p.Phe259Ser
|
|
NR_049782.1:n.1149T>C
|
|
|
NR_049783.1:n.1122T>C
|
|
|
NR_049784.1:n.1098T>C
|
|
|
NR_049785.1:n.1031T>C
|
|
|
NR_049786.1:n.980T>C
|
|
|
NR_049787.1:n.831T>C
|
|
|
NR_049788.1:n.761T>C
|
|
|
XM_011533203.1:c.134T>C
|
XP_011531505.1:p.Phe45Ser
|
|
XM_011533203.2:c.134T>C
|
XP_011531505.1:p.Phe45Ser
|
|
XM_017005405.2:c.134T>C
|
XP_016860894.1:p.Phe45Ser
|
|
NM_014748.4:c.776T>C
MANE Select
|
NP_055563.1:p.Phe259Ser
|
|
NM_001267059.2:c.740T>C
|
NP_001253988.1:p.Phe247Ser
|
|
NM_001267061.2:c.716T>C
|
NP_001253990.1:p.Phe239Ser
|
|
NR_049782.2:n.1029T>C
|
|
|
NR_049783.2:n.1002T>C
|
|
|
NR_049784.2:n.978T>C
|
|
|
NR_049785.2:n.911T>C
|
|
|
NR_049786.2:n.860T>C
|
|
|
NR_049787.2:n.711T>C
|
|
|
NR_049788.2:n.641T>C
|
|
|
NM_001267060.2:c.701T>C
|
NP_001253989.1:p.Phe234Ser
|
|