ENST00000233575.7:c.802C>T
MANE Select
|
ENSP00000233575.2:p.His268Tyr
|
|
ENST00000233575.6:c.802C>T
|
ENSP00000233575.2:p.His268Tyr
|
|
ENST00000427123.5:c.*612C>T
|
ENSP00000405399.1:n.*612C>T
|
|
ENST00000440760.5:c.*647C>T
|
ENSP00000399727.1:n.*647C>T
|
|
ENST00000453453.1:c.*329C>T
|
ENSP00000401922.1:n.*329C>T
|
|
ENST00000493711.1:n.519C>T
|
|
|
ENST00000537606.5:c.727C>T
|
ENSP00000439208.1:p.His243Tyr
|
|
NM_001267059.1:c.766C>T
|
NP_001253988.1:p.His256Tyr
|
|
NM_001267060.1:c.727C>T
|
NP_001253989.1:p.His243Tyr
|
|
NM_001267061.1:c.742C>T
|
NP_001253990.1:p.His248Tyr
|
|
NM_014748.3:c.802C>T
|
NP_055563.1:p.His268Tyr
|
|
NR_049782.1:n.1175C>T
|
|
|
NR_049783.1:n.1148C>T
|
|
|
NR_049784.1:n.1124C>T
|
|
|
NR_049785.1:n.1057C>T
|
|
|
NR_049786.1:n.1006C>T
|
|
|
NR_049787.1:n.857C>T
|
|
|
NR_049788.1:n.787C>T
|
|
|
XM_011533203.1:c.160C>T
|
XP_011531505.1:p.His54Tyr
|
|
XM_011533203.2:c.160C>T
|
XP_011531505.1:p.His54Tyr
|
|
XM_017005405.2:c.160C>T
|
XP_016860894.1:p.His54Tyr
|
|
NM_014748.4:c.802C>T
MANE Select
|
NP_055563.1:p.His268Tyr
|
|
NM_001267059.2:c.766C>T
|
NP_001253988.1:p.His256Tyr
|
|
NM_001267061.2:c.742C>T
|
NP_001253990.1:p.His248Tyr
|
|
NR_049782.2:n.1055C>T
|
|
|
NR_049783.2:n.1028C>T
|
|
|
NR_049784.2:n.1004C>T
|
|
|
NR_049785.2:n.937C>T
|
|
|
NR_049786.2:n.886C>T
|
|
|
NR_049787.2:n.737C>T
|
|
|
NR_049788.2:n.667C>T
|
|
|
NM_001267060.2:c.727C>T
|
NP_001253989.1:p.His243Tyr
|
|