ENST00000424685.3:c.226+1542G>A
|
ENSP00000388446.3:n.226+1542G>A
|
|
ENST00000428762.6:c.226+1542G>A
MANE Select
|
ENSP00000392423.1:n.226+1542G>A
|
|
ENST00000473457.2:n.490+1542G>A
|
|
|
ENST00000679689.1:n.386+1542G>A
|
|
|
ENST00000679867.1:n.110+1542G>A
|
|
|
ENST00000680712.1:n.40+1542G>A
|
|
|
ENST00000681034.1:c.226+1542G>A
|
ENSP00000506075.1:n.226+1542G>A
|
|
ENST00000681182.1:n.477+1542G>A
|
|
|
ENST00000681401.1:n.502+1542G>A
|
|
|
ENST00000681931.1:n.110+1542G>A
|
|
|
ENST00000343529.9:c.226+1542G>A
|
ENSP00000345694.5:n.226+1542G>A
|
|
ENST00000424685.2:c.226+1542G>A
|
ENSP00000388446.2:n.226+1542G>A
|
|
ENST00000428762.5:c.226+1542G>A
|
ENSP00000392423.1:n.226+1542G>A
|
|
NM_005045.3:c.226+1542G>A
|
NP_005036.2:n.226+1542G>A
|
|
NM_173054.2:c.226+1542G>A
|
NP_774959.1:n.226+1542G>A
|
|
NM_005045.4:c.226+1542G>A
MANE Select
|
NP_005036.2:n.226+1542G>A
|
|
NM_173054.3:c.226+1542G>A
|
NP_774959.1:n.226+1542G>A
|
|