ENST00000377636.8:c.2593+41T>C
MANE Select
|
ENSP00000366863.3:n.2593+41T>C
|
|
ENST00000648194.1:c.1861+41T>C
|
ENSP00000496983.1:n.1861+41T>C
|
|
ENST00000377625.6:c.2404+41T>C
|
ENSP00000366852.2:n.2404+41T>C
|
|
ENST00000377636.7:c.2593+41T>C
|
ENSP00000366863.3:n.2593+41T>C
|
|
ENST00000431480.6:c.2569+41T>C
|
ENSP00000395986.2:n.2569+41T>C
|
|
ENST00000493487.1:n.452+41T>C
|
|
|
NM_001286658.1:c.2569+41T>C
|
NP_001273587.1:n.2569+41T>C
|
|
NM_001286658.2:c.2569+41T>C
|
NP_001273587.1:n.2569+41T>C
|
|
NM_001286659.1:c.2404+41T>C
|
NP_001273588.1:n.2404+41T>C
|
|
NM_001286659.2:c.2404+41T>C
|
NP_001273588.1:n.2404+41T>C
|
|
NM_014832.3:c.2593+41T>C
|
NP_055647.2:n.2593+41T>C
|
|
NM_014832.4:c.2593+41T>C
|
NP_055647.2:n.2593+41T>C
|
|
XM_005266603.1:c.2518+41T>C
|
XP_005266660.1:n.2518+41T>C
|
|
XM_005266605.1:c.2050+41T>C
|
XP_005266662.1:n.2050+41T>C
|
|
XM_006719903.2:c.2119+41T>C
|
XP_006719966.1:n.2119+41T>C
|
|
XM_011535331.1:c.2482+41T>C
|
XP_011533633.1:n.2482+41T>C
|
|
XM_005266603.2:c.2518+41T>C
|
XP_005266660.1:n.2518+41T>C
|
|
XM_005266605.3:c.2050+41T>C
|
XP_005266662.1:n.2050+41T>C
|
|
XM_006719903.3:c.2119+41T>C
|
XP_006719966.1:n.2119+41T>C
|
|
XM_011535331.2:c.2482+41T>C
|
XP_011533633.1:n.2482+41T>C
|
|
XM_017020882.2:c.1861+41T>C
|
XP_016876371.1:n.1861+41T>C
|
|
XM_017020883.2:c.1750+41T>C
|
XP_016876372.1:n.1750+41T>C
|
|
XM_017020884.2:c.160+41T>C
|
XP_016876373.1:n.160+41T>C
|
|
NM_014832.5:c.2593+41T>C
MANE Select
|
NP_055647.2:n.2593+41T>C
|
|