ENST00000327097.5:c.613+807G>A
MANE Select
|
ENSP00000318916.4:n.613+807G>A
|
|
ENST00000327097.4:c.613+807G>A
|
ENSP00000318916.4:n.613+807G>A
|
|
NM_006770.3:c.613+807G>A
|
NP_006761.1:n.613+807G>A
|
|
XM_011512082.1:c.613+807G>A
|
XP_011510384.1:n.613+807G>A
|
|
XM_011512083.1:c.250+807G>A
|
XP_011510385.1:n.250+807G>A
|
|
XM_011512082.2:c.613+807G>A
|
XP_011510384.1:n.613+807G>A
|
|
XM_011512083.3:c.250+807G>A
|
XP_011510385.1:n.250+807G>A
|
|
XM_017005171.2:c.613+807G>A
|
XP_016860660.1:n.613+807G>A
|
|
NM_006770.4:c.613+807G>A
MANE Select
|
NP_006761.1:n.613+807G>A
|
|