ENST00000378802.5:c.988-585G>T
MANE Select
|
ENSP00000368079.4:n.988-585G>T
|
|
ENST00000378802.4:c.988-585G>T
|
ENSP00000368079.4:n.988-585G>T
|
|
ENST00000507209.5:n.5101G>T
|
|
|
ENST00000513354.5:n.77+158G>T
|
|
|
NM_207352.3:c.988-585G>T
|
NP_997235.3:n.988-585G>T
|
|
XM_005262935.2:c.988-585G>T
|
XP_005262992.1:n.988-585G>T
|
|
XM_006714184.2:c.592-585G>T
|
XP_006714247.1:n.592-585G>T
|
|
XM_005262935.4:c.988-585G>T
|
XP_005262992.1:n.988-585G>T
|
|
XM_017008037.1:c.592-585G>T
|
XP_016863526.1:n.592-585G>T
|
|
NM_207352.4:c.988-585G>T
MANE Select
|
NP_997235.3:n.988-585G>T
|
|