ENST00000455146.8:c.898C>T
MANE Select
|
ENSP00000397441.2:p.His300Tyr
|
|
ENST00000356576.8:c.*735C>T
|
ENSP00000348983.4:n.*735C>T
|
|
ENST00000416691.5:c.898C>T
|
ENSP00000403733.1:p.His300Tyr
|
|
ENST00000455146.7:c.898C>T
|
ENSP00000397441.2:p.His300Tyr
|
|
ENST00000460701.1:n.70C>T
|
|
|
NM_001145079.1:c.898C>T
|
NP_001138551.1:p.His300Tyr
|
|
NM_020751.2:c.898C>T
|
NP_065802.1:p.His300Tyr
|
|
NR_026745.1:n.1063C>T
|
|
|
XM_011535168.1:c.898C>T
|
XP_011533470.1:p.His300Tyr
|
|
XM_011535169.1:c.742C>T
|
XP_011533471.1:p.His248Tyr
|
|
XM_011535170.1:c.742C>T
|
XP_011533472.1:p.His248Tyr
|
|
NM_020751.3:c.898C>T
MANE Select
|
NP_065802.1:p.His300Tyr
|
|
NM_001145079.2:c.898C>T
|
NP_001138551.1:p.His300Tyr
|
|