ENST00000375708.4:c.2804A>T
MANE Select
|
ENSP00000364860.3:p.Asp935Val
|
|
ENST00000375708.3:c.2804A>T
|
ENSP00000364860.3:p.Asp935Val
|
|
ENST00000375715.5:c.1920+464A>T
|
ENSP00000364867.1:n.1920+464A>T
|
|
ENST00000550066.5:n.3272A>T
|
|
|
NM_004560.3:c.2804A>T
|
NP_004551.2:p.Asp935Val
|
|
XM_005252008.3:c.2384A>T
|
XP_005252065.1:p.Asp795Val
|
|
XM_005252009.3:c.1601A>T
|
XP_005252066.1:p.Asp534Val
|
|
XM_006717121.2:c.2384A>T
|
XP_006717184.1:p.Asp795Val
|
|
XM_011518721.1:c.2384A>T
|
XP_011517023.1:p.Asp795Val
|
|
XM_005252008.4:c.2384A>T
|
XP_005252065.1:p.Asp795Val
|
|
XM_006717121.3:c.2384A>T
|
XP_006717184.1:p.Asp795Val
|
|
XM_017014762.1:c.2795A>T
|
XP_016870251.1:p.Asp932Val
|
|
XM_017014763.1:c.2384A>T
|
XP_016870252.1:p.Asp795Val
|
|
NM_004560.4:c.2804A>T
MANE Select
|
NP_004551.2:p.Asp935Val
|
|