ENST00000301305.8:c.977-8G>T
MANE Select
|
ENSP00000301305.4:n.977-8G>T
|
|
ENST00000276833.9:c.902-8G>T
|
ENSP00000276833.5:n.902-8G>T
|
|
ENST00000301305.7:c.977-8G>T
|
ENSP00000301305.3:n.977-8G>T
|
|
NM_017767.2:c.902-8G>T
|
NP_060237.2:n.902-8G>T
|
|
NM_130849.3:c.977-8G>T
|
NP_570901.2:n.977-8G>T
|
|
XM_006716599.1:c.977-8G>T
|
XP_006716662.1:n.977-8G>T
|
|
XM_011517153.1:c.695-8G>T
|
XP_011515455.1:n.695-8G>T
|
|
XM_024447188.1:c.695-8G>T
|
XP_024302956.1:n.695-8G>T
|
|
XM_024447189.1:c.695-8G>T
|
XP_024302957.1:n.695-8G>T
|
|
NM_001374839.1:c.695-8G>T
|
NP_001361768.1:n.695-8G>T
|
|
NM_017767.3:c.902-8G>T
|
NP_060237.3:n.902-8G>T
|
|
NM_130849.4:c.977-8G>T
MANE Select
|
NP_570901.3:n.977-8G>T
|
|