ENST00000242317.9:c.1606T>C
MANE Select
|
ENSP00000242317.4:p.Tyr536His
|
|
ENST00000242317.8:c.1606T>C
|
ENSP00000242317.4:p.Tyr536His
|
|
ENST00000442556.1:c.117T>C
|
|
|
ENST00000470169.5:c.507-210T>C
|
|
|
ENST00000485580.1:n.85T>C
|
|
|
ENST00000614641.4:c.1618T>C
|
ENSP00000480538.1:p.Tyr540His
|
|
NM_001281428.1:c.1618T>C
|
NP_001268357.1:p.Tyr540His
|
|
NM_012144.3:c.1606T>C
|
NP_036276.1:p.Tyr536His
|
|
XM_006716758.2:c.1075T>C
|
XP_006716821.1:p.Tyr359His
|
|
XM_011517846.1:c.1618T>C
|
XP_011516148.1:p.Tyr540His
|
|
XM_011517847.1:c.1618T>C
|
XP_011516149.1:p.Tyr540His
|
|
XM_011517848.1:c.1360T>C
|
XP_011516150.1:p.Tyr454His
|
|
XM_011517849.1:c.1582-74T>C
|
XP_011516151.1:n.1582-74T>C
|
|
XR_929232.1:n.1836-74T>C
|
|
|
XR_929233.1:n.1836-74T>C
|
|
|
XR_929235.1:n.1578-74T>C
|
|
|
XM_006716758.3:c.1075T>C
|
XP_006716821.1:p.Tyr359His
|
|
XM_011517846.2:c.1618T>C
|
XP_011516148.1:p.Tyr540His
|
|
XM_011517847.3:c.1618T>C
|
XP_011516149.1:p.Tyr540His
|
|
XM_011517848.2:c.1360T>C
|
XP_011516150.1:p.Tyr454His
|
|
XM_011517849.2:c.1582-74T>C
|
XP_011516151.1:n.1582-74T>C
|
|
XM_017014625.2:c.1348T>C
|
XP_016870114.1:p.Tyr450His
|
|
XR_002956774.1:n.1783-74T>C
|
|
|
XR_929232.2:n.1783-74T>C
|
|
|
XR_929233.2:n.1783-74T>C
|
|
|
NM_012144.4:c.1606T>C
MANE Select
|
NP_036276.1:p.Tyr536His
|
|
NM_001281428.2:c.1618T>C
|
NP_001268357.1:p.Tyr540His
|
|