ENST00000262493.12:c.877+69G>T
MANE Select
|
ENSP00000262493.6:n.877+69G>T
|
|
ENST00000562316.6:c.544+69G>T
|
ENSP00000457238.2:n.544+69G>T
|
|
ENST00000564727.2:c.181+69G>T
|
ENSP00000454971.2:n.181+69G>T
|
|
ENST00000568375.2:c.116-3260G>T
|
|
|
ENST00000638185.1:n.1092+69G>T
|
|
|
ENST00000638210.1:n.1177+69G>T
|
|
|
ENST00000638705.1:c.877+69G>T
|
ENSP00000491223.1:n.877+69G>T
|
|
ENST00000638836.1:n.787+69G>T
|
|
|
ENST00000639055.1:n.1598+69G>T
|
|
|
ENST00000639251.1:n.778+69G>T
|
|
|
ENST00000639268.1:c.512+69G>T
|
|
|
ENST00000639341.1:c.402+69G>T
|
|
|
ENST00000639770.1:c.915+69G>T
|
ENSP00000491999.1:n.915+69G>T
|
|
ENST00000640390.1:n.807+69G>T
|
|
|
ENST00000640469.1:c.241+69G>T
|
ENSP00000491875.1:n.241+69G>T
|
|
ENST00000640560.1:n.653+69G>T
|
|
|
ENST00000640893.1:c.*275+69G>T
|
ENSP00000492677.1:n.*275+69G>T
|
|
ENST00000262493.10:c.877+69G>T
|
ENSP00000262493.6:n.877+69G>T
|
|
ENST00000564727.1:c.97+69G>T
|
ENSP00000454971.1:n.97+69G>T
|
|
ENST00000568375.1:n.116-3260G>T
|
|
|
NM_020988.2:c.877+69G>T
|
NP_066268.1:n.877+69G>T
|
|
XM_011523003.1:c.751+69G>T
|
XP_011521305.1:n.751+69G>T
|
|
XM_011523003.3:c.751+69G>T
|
XP_011521305.1:n.751+69G>T
|
|
NM_020988.3:c.877+69G>T
MANE Select
|
NP_066268.1:n.877+69G>T
|
|