ENST00000330342.8:c.1189+19A>G
MANE Select
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ENSP00000332247.2:n.1189+19A>G
|
|
ENST00000540368.6:n.1220+19A>G
|
|
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ENST00000674794.1:c.1277+19A>G
|
|
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ENST00000675260.1:n.464+19A>G
|
|
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ENST00000675344.1:c.*210+19A>G
|
ENSP00000501953.1:n.*210+19A>G
|
|
ENST00000330342.7:c.1189+19A>G
|
ENSP00000332247.2:n.1189+19A>G
|
|
ENST00000504192.2:c.799+19A>G
|
ENSP00000443441.1:n.799+19A>G
|
|
ENST00000536426.1:n.206+19A>G
|
|
|
ENST00000545059.5:n.3825+19A>G
|
|
|
NM_012463.3:c.1189+19A>G
|
NP_036595.2:n.1189+19A>G
|
|
XM_005253563.1:c.1189+19A>G
|
XP_005253620.1:n.1189+19A>G
|
|
XM_006719317.2:c.676+19A>G
|
XP_006719380.1:n.676+19A>G
|
|
XM_006719318.2:c.367+19A>G
|
XP_006719381.1:n.367+19A>G
|
|
XR_429088.1:n.1352+19A>G
|
|
|
XM_024448910.1:c.1189+19A>G
|
XP_024304678.1:n.1189+19A>G
|
|
XM_024448911.1:c.676+19A>G
|
XP_024304679.1:n.676+19A>G
|
|
XM_024448912.1:c.367+19A>G
|
XP_024304680.1:n.367+19A>G
|
|
NM_012463.4:c.1189+19A>G
MANE Select
|
NP_036595.2:n.1189+19A>G
|
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