ENST00000327097.5:c.98-945G>A
MANE Select
|
ENSP00000318916.4:n.98-945G>A
|
|
ENST00000327097.4:c.98-945G>A
|
ENSP00000318916.4:n.98-945G>A
|
|
ENST00000412481.1:c.-137-945G>A
|
ENSP00000409192.1:n.-137-945G>A
|
|
NM_006770.3:c.98-945G>A
|
NP_006761.1:n.98-945G>A
|
|
XM_011512082.1:c.98-945G>A
|
XP_011510384.1:n.98-945G>A
|
|
XM_011512083.1:c.98-6118G>A
|
XP_011510385.1:n.98-6118G>A
|
|
XM_011512082.2:c.98-945G>A
|
XP_011510384.1:n.98-945G>A
|
|
XM_011512083.3:c.98-6118G>A
|
XP_011510385.1:n.98-6118G>A
|
|
XM_017005171.2:c.98-945G>A
|
XP_016860660.1:n.98-945G>A
|
|
NM_006770.4:c.98-945G>A
MANE Select
|
NP_006761.1:n.98-945G>A
|
|