ENST00000261769.10:c.2164+10G>T
MANE Select
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ENSP00000261769.4:n.2164+10G>T
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ENST00000261769.9:c.2164+10G>T
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ENSP00000261769.4:n.2164+10G>T
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ENST00000422392.6:c.1981+10G>T
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ENSP00000414946.2:n.1981+10G>T
|
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ENST00000562118.1:n.382+10G>T
|
|
|
ENST00000562836.5:n.2235+10G>T
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|
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ENST00000566510.5:c.*830+10G>T
|
ENSP00000458139.1:n.*830+10G>T
|
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ENST00000566612.5:c.*404+10G>T
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ENSP00000454782.1:n.*404+10G>T
|
|
ENST00000611625.4:c.2227+10G>T
|
ENSP00000481063.1:n.2227+10G>T
|
|
ENST00000612417.4:c.1830+1517G>T
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ENSP00000478360.1:n.1830+1517G>T
|
|
ENST00000621016.4:c.1865+1482G>T
|
ENSP00000480664.1:n.1865+1482G>T
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|
NM_004360.3:c.2164+10G>T , LRG_301t1:c.2164+10G>T
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NP_004351.1:n.2164+10G>T
|
|
XM_011523488.1:c.1429+10G>T
|
XP_011521790.1:n.1429+10G>T
|
|
XM_011523489.1:c.1429+10G>T
|
XP_011521791.1:n.1429+10G>T
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NM_001317184.1:c.1981+10G>T
|
NP_001304113.1:n.1981+10G>T
|
|
NM_001317185.1:c.616+10G>T
|
NP_001304114.1:n.616+10G>T
|
|
NM_001317186.1:c.199+10G>T
|
NP_001304115.1:n.199+10G>T
|
|
NM_004360.4:c.2164+10G>T
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NP_004351.1:n.2164+10G>T
|
|
NM_004360.5:c.2164+10G>T
MANE Select
|
NP_004351.1:n.2164+10G>T
|
|
NM_001317184.2:c.1981+10G>T
|
NP_001304113.1:n.1981+10G>T
|
|
NM_001317185.2:c.616+10G>T
|
NP_001304114.1:n.616+10G>T
|
|
NM_001317186.2:c.199+10G>T
|
NP_001304115.1:n.199+10G>T
|
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