|
NM_001851.6:c.2112+115dup
MANE Select
|
NP_001842.3:n.2112+115dup
|
|
ENST00000357250.11:c.2112+115dup
MANE Select
|
ENSP00000349790.6:n.2112+115dup
|
|
NM_001377289.1:c.1413+115dup
|
NP_001364218.1:n.1413+115dup
|
|
NM_001377290.1:c.1383+115dup
|
NP_001364219.1:n.1383+115dup
|
|
NM_001851.4:c.2112+115dup
|
NP_001842.3:n.2112+115dup
|
|
NM_001851.5:c.2112+115dup
|
NP_001842.3:n.2112+115dup
|
|
NM_078485.3:c.1383+115dup
|
NP_511040.2:n.1383+115dup
|
|
NM_078485.4:c.1383+115dup
|
NP_511040.2:n.1383+115dup
|
|
NR_165185.1:n.1633+115dup
|
|
|
ENST00000320755.11:c.1383+115dup
|
ENSP00000315252.7:n.1383+115dup
|
|
ENST00000320755.12:c.1383+115dup
|
ENSP00000315252.7:n.1383+115dup
|
|
ENST00000357250.10:c.2112+115dup
|
ENSP00000349790.6:n.2112+115dup
|
|
ENST00000360859.11:n.798+115dup
|
|
|
ENST00000360859.12:n.798+115dup
|
|
|
ENST00000447041.6:n.509+115dup
|
|
|
ENST00000486080.5:n.817+115dup
|
|
|
ENST00000489611.5:n.1132+115dup
|
|
|
ENST00000493682.6:n.1085+115dup
|
|
|
ENST00000493682.7:n.2106+115dup
|
|
|
ENST00000644493.1:c.*1149+115dup
|
ENSP00000495638.1:n.*1149+115dup
|
|
ENST00000683602.1:n.2849+115dup
|
|
|
ENST00000683758.1:c.1392+106dup
|
ENSP00000508147.1:n.1392+106dup
|
|
ENST00000683980.1:c.1413+115dup
|
ENSP00000506990.1:n.1413+115dup
|
|
ENST00000683980.2:c.1413+115dup
|
ENSP00000506990.1:n.1413+115dup
|
|
ENST00000684176.1:n.1454+115dup
|
|
|
XM_011535429.1:c.2142+115dup
|
XP_011533731.1:n.2142+115dup
|
|
XM_011535429.3:c.2142+115dup
|
XP_011533731.1:n.2142+115dup
|
|
XM_011535430.1:c.1413+115dup
|
XP_011533732.1:n.1413+115dup
|
|
XM_011535430.3:c.1413+115dup
|
XP_011533732.1:n.1413+115dup
|
|
XM_011535431.1:c.804+115dup
|
XP_011533733.1:n.804+115dup
|
|
XM_017010246.2:c.1593+115dup
|
XP_016865735.1:n.1593+115dup
|
|
XM_017010247.2:c.861+115dup
|
XP_016865736.1:n.861+115dup
|
