ENST00000389048.8:c.3515+177T>C
MANE Select
|
ENSP00000373700.3:n.3515+177T>C
|
|
ENST00000431873.6:c.742+177T>C
|
|
|
ENST00000638605.1:n.392+177T>C
|
|
|
ENST00000642122.1:c.311+177T>C
|
ENSP00000493203.1:n.311+177T>C
|
|
ENST00000389048.7:c.3515+177T>C
|
ENSP00000373700.3:n.3515+177T>C
|
|
ENST00000431873.5:c.395+177T>C
|
ENSP00000414027.2:n.395+177T>C
|
|
ENST00000453137.1:c.209+177T>C
|
ENSP00000387488.1:n.209+177T>C
|
|
ENST00000618119.4:c.2384+177T>C
|
ENSP00000482733.1:n.2384+177T>C
|
|
NM_004304.4:c.3515+177T>C
|
NP_004295.2:n.3515+177T>C
|
|
NM_001353765.1:c.311+177T>C
|
NP_001340694.1:n.311+177T>C
|
|
XM_024452778.1:c.668+177T>C
|
XP_024308546.1:n.668+177T>C
|
|
XM_024452779.1:c.311+177T>C
|
XP_024308547.1:n.311+177T>C
|
|
NM_004304.5:c.3515+177T>C
MANE Select
|
NP_004295.2:n.3515+177T>C
|
|
NM_001353765.2:c.311+177T>C
|
NP_001340694.1:n.311+177T>C
|
|