ENST00000220616.9:c.8051C>A
MANE Select
|
ENSP00000220616.4:p.Pro2684His
|
|
ENST00000220616.8:c.8051C>A
|
ENSP00000220616.4:p.Pro2684His
|
|
ENST00000519178.5:c.3417C>A
|
|
|
ENST00000519543.5:c.2450C>A
|
ENSP00000430430.1:p.Pro817His
|
|
ENST00000521107.1:c.263C>A
|
ENSP00000430161.1:p.Pro88His
|
|
ENST00000522691.1:n.137C>A
|
|
|
ENST00000523756.5:c.4706C>A
|
|
|
NM_003235.4:c.8051C>A
|
NP_003226.4:p.Pro2684His
|
|
XM_005251038.3:c.7859C>A
|
XP_005251095.1:p.Pro2620His
|
|
XM_006716622.2:c.7988C>A
|
XP_006716685.1:p.Pro2663His
|
|
XM_005251038.4:c.7859C>A
|
XP_005251095.1:p.Pro2620His
|
|
XM_006716622.3:c.7988C>A
|
XP_006716685.1:p.Pro2663His
|
|
XM_017013793.1:c.7985C>A
|
XP_016869282.1:p.Pro2662His
|
|
XM_017013794.1:c.7916C>A
|
XP_016869283.1:p.Pro2639His
|
|
XM_017013795.1:c.7880C>A
|
XP_016869284.1:p.Pro2627His
|
|
XM_017013796.1:c.7832C>A
|
XP_016869285.1:p.Pro2611His
|
|
XM_017013797.1:c.7790C>A
|
XP_016869286.1:p.Pro2597His
|
|
NM_003235.5:c.8051C>A
MANE Select
|
NP_003226.4:p.Pro2684His
|
|