ENST00000378585.7:c.69-339G>T
MANE Select
|
ENSP00000367848.4:n.69-339G>T
|
|
ENST00000638411.1:c.69-339G>T
|
ENSP00000491632.1:n.69-339G>T
|
|
ENST00000638604.1:n.133-339G>T
|
|
|
ENST00000638771.1:c.69-339G>T
|
ENSP00000492435.1:n.69-339G>T
|
|
ENST00000639045.1:c.*55-339G>T
|
ENSP00000491997.1:n.*55-339G>T
|
|
ENST00000639777.1:n.334G>T
|
|
|
ENST00000639935.1:n.106-339G>T
|
|
|
ENST00000640030.1:c.9-339G>T
|
ENSP00000491411.1:n.9-339G>T
|
|
ENST00000640067.1:c.69-339G>T
|
ENSP00000491844.1:n.69-339G>T
|
|
ENST00000640423.1:n.78-339G>T
|
|
|
ENST00000640949.1:c.69-339G>T
|
ENSP00000492500.1:n.69-339G>T
|
|
ENST00000378585.5:c.69-339G>T
|
ENSP00000367848.4:n.69-339G>T
|
|
NM_000815.4:c.69-339G>T
|
NP_000806.2:n.69-339G>T
|
|
XM_011541194.1:c.108-339G>T
|
XP_011539496.1:n.108-339G>T
|
|
XM_011541194.3:c.108-339G>T
|
XP_011539496.1:n.108-339G>T
|
|
XM_017000936.1:c.435G>T
|
XP_016856425.1:p.Leu145Phe
|
|
NM_000815.5:c.69-339G>T
MANE Select
|
NP_000806.2:n.69-339G>T
|
|