ENST00000220616.9:c.8036C>A
MANE Select
|
ENSP00000220616.4:p.Pro2679His
|
|
ENST00000220616.8:c.8036C>A
|
ENSP00000220616.4:p.Pro2679His
|
|
ENST00000519178.5:c.3402C>A
|
|
|
ENST00000519543.5:c.2435C>A
|
ENSP00000430430.1:p.Pro812His
|
|
ENST00000521107.1:c.248C>A
|
ENSP00000430161.1:p.Pro83His
|
|
ENST00000522691.1:n.122C>A
|
|
|
ENST00000523756.5:c.4691C>A
|
|
|
NM_003235.4:c.8036C>A
|
NP_003226.4:p.Pro2679His
|
|
XM_005251038.3:c.7844C>A
|
XP_005251095.1:p.Pro2615His
|
|
XM_006716622.2:c.7973C>A
|
XP_006716685.1:p.Pro2658His
|
|
XM_005251038.4:c.7844C>A
|
XP_005251095.1:p.Pro2615His
|
|
XM_006716622.3:c.7973C>A
|
XP_006716685.1:p.Pro2658His
|
|
XM_017013793.1:c.7970C>A
|
XP_016869282.1:p.Pro2657His
|
|
XM_017013794.1:c.7901C>A
|
XP_016869283.1:p.Pro2634His
|
|
XM_017013795.1:c.7865C>A
|
XP_016869284.1:p.Pro2622His
|
|
XM_017013796.1:c.7817C>A
|
XP_016869285.1:p.Pro2606His
|
|
XM_017013797.1:c.7775C>A
|
XP_016869286.1:p.Pro2592His
|
|
NM_003235.5:c.8036C>A
MANE Select
|
NP_003226.4:p.Pro2679His
|
|