ENST00000359151.8:c.*517A>T
MANE Select
|
ENSP00000352064.3:n.*517A>T
|
|
ENST00000347831.9:c.*517A>T
|
ENSP00000256965.7:n.*517A>T
|
|
ENST00000359151.7:c.*517A>T
|
ENSP00000352064.3:n.*517A>T
|
|
ENST00000408006.7:c.*517A>T
|
ENSP00000385304.3:n.*517A>T
|
|
ENST00000536188.5:c.685+534A>T
|
ENSP00000441432.1:n.685+534A>T
|
|
NM_001304448.1:c.685+534A>T
|
NP_001291377.1:n.685+534A>T
|
|
NM_002259.4:c.*517A>T
|
NP_002250.1:n.*517A>T
|
|
NM_007328.3:c.*517A>T
|
NP_015567.1:n.*517A>T
|
|
NM_213657.2:c.*517A>T
|
NP_998822.1:n.*517A>T
|
|
NM_213658.2:c.*517A>T
|
NP_998823.1:n.*517A>T
|
|
XM_024448973.1:c.685+534A>T
|
XP_024304741.1:n.685+534A>T
|
|
NM_002259.5:c.*517A>T
MANE Select
|
NP_002250.2:n.*517A>T
|
|
NM_007328.4:c.*517A>T
|
NP_015567.2:n.*517A>T
|
|
NM_213657.3:c.*517A>T
|
NP_998822.2:n.*517A>T
|
|
NM_213658.3:c.*517A>T
|
NP_998823.2:n.*517A>T
|
|