ENST00000372470.9:c.391+5G>T
MANE Select
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ENSP00000361548.3:n.391+5G>T
|
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ENST00000413998.7:c.370+5G>T
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ENSP00000414004.3:n.370+5G>T
|
|
ENST00000638732.1:n.391+5G>T
|
|
|
ENST00000372470.7:c.391+5G>T
|
ENSP00000361548.3:n.391+5G>T
|
|
ENST00000413998.6:c.391+5G>T
|
ENSP00000414004.2:n.391+5G>T
|
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ENST00000612993.1:c.391+5G>T
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ENSP00000480273.1:n.391+5G>T
|
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NM_005373.2:c.391+5G>T , LRG_510t1:c.391+5G>T
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NP_005364.1:n.391+5G>T
|
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XM_011541478.1:c.370+5G>T
|
XP_011539780.1:n.370+5G>T
|
|
XM_017001320.1:c.562+5G>T
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XP_016856809.1:n.562+5G>T
|
|
NM_005373.3:c.391+5G>T
MANE Select
|
NP_005364.1:n.391+5G>T
|
|