ENST00000450053.8:c.1899-39G>A
MANE Select
|
ENSP00000415034.2:n.1899-39G>A
|
|
ENST00000651747.1:c.1797-39G>A
|
ENSP00000499216.1:n.1797-39G>A
|
|
ENST00000416683.5:c.314-39G>A
|
|
|
ENST00000450053.7:c.1899-39G>A
|
ENSP00000415034.2:n.1899-39G>A
|
|
NM_015175.2:c.1899-39G>A , LRG_568t1:c.1899-39G>A
|
NP_055990.1:n.1899-39G>A
|
|
XM_005264992.2:c.1797-39G>A
|
XP_005265049.1:n.1797-39G>A
|
|
XM_006713072.2:c.1818-39G>A
|
XP_006713135.1:n.1818-39G>A
|
|
XM_011533532.1:c.1878-39G>A
|
XP_011531834.1:n.1878-39G>A
|
|
XM_011533533.1:c.1899-39G>A
|
XP_011531835.1:n.1899-39G>A
|
|
XM_011533534.1:c.1530-39G>A
|
XP_011531836.1:n.1530-39G>A
|
|
XM_011533535.1:c.1359-39G>A
|
XP_011531837.1:n.1359-39G>A
|
|
XM_011533536.1:c.1245-39G>A
|
XP_011531838.1:n.1245-39G>A
|
|
XM_011533537.1:c.807-39G>A
|
XP_011531839.1:n.807-39G>A
|
|
XR_940397.1:n.2075-39G>A
|
|
|
XR_940398.1:n.2075-39G>A
|
|
|
NM_001365116.1:c.1797-39G>A
|
NP_001352045.1:n.1797-39G>A
|
|
XM_006713072.3:c.1818-39G>A
|
XP_006713135.1:n.1818-39G>A
|
|
XM_011533533.2:c.1899-39G>A
|
XP_011531835.1:n.1899-39G>A
|
|
XM_017006010.1:c.1899-39G>A
|
XP_016861499.1:n.1899-39G>A
|
|
XM_017006011.1:c.1878-39G>A
|
XP_016861500.1:n.1878-39G>A
|
|
XM_017006012.1:c.1818-39G>A
|
XP_016861501.1:n.1818-39G>A
|
|
XM_017006013.1:c.1899-39G>A
|
XP_016861502.1:n.1899-39G>A
|
|
XM_017006014.1:c.1797-39G>A
|
XP_016861503.1:n.1797-39G>A
|
|
XM_017006015.1:c.1530-39G>A
|
XP_016861504.1:n.1530-39G>A
|
|
XM_017006016.1:c.1359-39G>A
|
XP_016861505.1:n.1359-39G>A
|
|
XR_940397.2:n.2075-39G>A
|
|
|
NM_001365116.2:c.1797-39G>A
|
NP_001352045.1:n.1797-39G>A
|
|
NM_015175.3:c.1899-39G>A
MANE Select
|
NP_055990.1:n.1899-39G>A
|
|