|
NM_001039141.3:c.5285C>T
MANE Select
|
NP_001034230.1:p.Pro1762Leu
|
|
ENST00000644935.1:c.5285C>T
MANE Select
|
ENSP00000496394.1:p.Pro1762Leu
|
|
NM_001039141.2:c.5285C>T
|
NP_001034230.1:p.Pro1762Leu
|
|
ENST00000344404.10:c.*4768C>T
|
ENSP00000340312.6:n.*4768C>T
|
|
ENST00000406386.7:c.5285C>T
|
ENSP00000384312.3:p.Pro1762Leu
|
|
XM_011530646.1:c.367-236G>A
|
XP_011528948.1:n.367-236G>A
|
|
XM_011530647.1:c.367-236G>A
|
XP_011528949.1:n.367-236G>A
|
|
XM_011530647.2:c.367-236G>A
|
XP_011528949.1:n.367-236G>A
|
|
XM_017029173.1:c.19-236G>A
|
XP_016884662.1:n.19-236G>A
|
|
XR_938241.1:n.361-236G>A
|
|
|
XR_938241.2:n.340-236G>A
|
|
|
XR_938242.1:n.314-236G>A
|
|