ENST00000308159.10:c.1899+108G>C
MANE Select
|
ENSP00000310668.5:n.1899+108G>C
|
|
ENST00000308159.9:c.1899+108G>C
|
ENSP00000310668.5:n.1899+108G>C
|
|
ENST00000542526.5:c.1530+108G>C
|
ENSP00000440235.1:n.1530+108G>C
|
|
ENST00000563405.1:c.93+108G>C
|
ENSP00000458078.1:n.93+108G>C
|
|
ENST00000564887.5:c.1530+108G>C
|
ENSP00000458039.1:n.1530+108G>C
|
|
ENST00000569842.5:c.1899+108G>C
|
ENSP00000458101.1:n.1899+108G>C
|
|
NM_001242795.1:c.1530+108G>C
|
NP_001229724.1:n.1530+108G>C
|
|
NM_001242796.1:c.1530+108G>C
|
NP_001229725.1:n.1530+108G>C
|
|
NM_014669.4:c.1899+108G>C
|
NP_055484.3:n.1899+108G>C
|
|
XM_005256263.2:c.1899+108G>C
|
XP_005256320.1:n.1899+108G>C
|
|
NM_001242796.2:c.1530+108G>C
|
NP_001229725.1:n.1530+108G>C
|
|
XM_005256263.3:c.1899+108G>C
|
XP_005256320.1:n.1899+108G>C
|
|
NM_014669.5:c.1899+108G>C
MANE Select
|
NP_055484.3:n.1899+108G>C
|
|
NM_001242795.2:c.1530+108G>C
|
NP_001229724.1:n.1530+108G>C
|
|