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ENSP00000485357.2:n.14838-396G>A
|
|
ENST00000683500.2:c.14895-396G>A
MANE Select
|
ENSP00000508292.2:n.14895-396G>A
|
|
ENST00000623487.1:n.2845G>A
|
|
|
ENST00000624552.3:c.14835-396G>A
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ENSP00000485357.1:n.14835-396G>A
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|
NM_001291815.1:c.14895-396G>A
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NP_001278744.1:n.14895-396G>A
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|
XM_011518465.1:c.14772-396G>A
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XP_011516767.1:n.14772-396G>A
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|
XM_011518466.1:c.14763-396G>A
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XP_011516768.1:n.14763-396G>A
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|
XM_011518467.1:c.14718-396G>A
|
XP_011516769.1:n.14718-396G>A
|
|
NM_001291815.2:c.14895-396G>A
MANE Select
|
NP_001278744.1:n.14895-396G>A
|
|
XM_011518465.2:c.14772-396G>A
|
XP_011516767.1:n.14772-396G>A
|
|
XM_011518466.2:c.14763-396G>A
|
XP_011516768.1:n.14763-396G>A
|
|
XM_011518467.2:c.14718-396G>A
|
XP_011516769.1:n.14718-396G>A
|
|
XM_017014585.1:c.11676-396G>A
|
XP_016870074.1:n.11676-396G>A
|
|
XM_017014586.1:c.7473-396G>A
|
XP_016870075.1:n.7473-396G>A
|
|
XR_001746957.1:n.92+669C>T
|
|
|
XR_001746958.1:n.92+669C>T
|
|
|