ENST00000424848.3:c.834+441G>C
MANE Select
|
ENSP00000397087.3:n.834+441G>C
|
|
ENST00000265734.8:c.834+441G>C
|
ENSP00000265734.4:n.834+441G>C
|
|
ENST00000424848.2:c.834+441G>C
|
ENSP00000397087.2:n.834+441G>C
|
|
ENST00000467166.1:n.206+441G>C
|
|
|
NM_001145306.1:c.834+441G>C
|
NP_001138778.1:n.834+441G>C
|
|
NM_001259.6:c.834+441G>C
|
NP_001250.1:n.834+441G>C
|
|
XM_006715835.1:c.834+441G>C
|
XP_006715898.1:n.834+441G>C
|
|
XM_011515731.1:c.834+441G>C
|
XP_011514033.1:n.834+441G>C
|
|
NM_001259.7:c.834+441G>C
|
NP_001250.1:n.834+441G>C
|
|
XM_006715835.2:c.834+441G>C
|
XP_006715898.1:n.834+441G>C
|
|
NM_001145306.2:c.834+441G>C
MANE Select
|
NP_001138778.1:n.834+441G>C
|
|
NM_001259.8:c.834+441G>C
|
NP_001250.1:n.834+441G>C
|
|