ENST00000225927.7:c.532-35G>T
MANE Select
|
ENSP00000225927.1:n.532-35G>T
|
|
ENST00000225927.6:c.532-35G>T
|
ENSP00000225927.1:n.532-35G>T
|
|
ENST00000586516.5:c.134-35G>T
|
|
|
ENST00000590358.1:c.220-35G>T
|
ENSP00000466892.1:n.220-35G>T
|
|
ENST00000591587.1:c.127-35G>T
|
ENSP00000467836.1:n.127-35G>T
|
|
NM_000263.3:c.532-35G>T
|
NP_000254.2:n.532-35G>T
|
|
XM_006721920.2:c.-211-35G>T
|
XP_006721983.1:n.-211-35G>T
|
|
XM_011524840.1:c.-211-35G>T
|
XP_011523142.1:n.-211-35G>T
|
|
XM_017024687.1:c.-211-35G>T
|
XP_016880176.1:n.-211-35G>T
|
|
XM_024450771.1:c.589-35G>T
|
XP_024306539.1:n.589-35G>T
|
|
XM_024450772.1:c.-211-35G>T
|
XP_024306540.1:n.-211-35G>T
|
|
NM_000263.4:c.532-35G>T
MANE Select
|
NP_000254.2:n.532-35G>T
|
|