ENST00000229771.11:c.1324-133_1324-132insCT
MANE Select
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ENSP00000229771.6:n.1324-133_1324-132insCT
|
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ENST00000229771.10:c.1324-133_1324-132insCT
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ENSP00000229771.6:n.1324-133_1324-132insCT
|
|
ENST00000322263.8:c.1165-133_1165-132insCT
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ENSP00000319414.4:n.1165-133_1165-132insCT
|
|
ENST00000495781.1:n.500-133_500-132insCT
|
|
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ENST00000614066.4:c.1318-133_1318-132insCT
|
ENSP00000477534.1:n.1318-133_1318-132insCT
|
|
NM_001289395.1:c.1165-133_1165-132insCT
|
NP_001276324.1:n.1165-133_1165-132insCT
|
|
NM_003322.4:c.1324-133_1324-132insCT
|
NP_003313.3:n.1324-133_1324-132insCT
|
|
NM_003322.5:c.1324-133_1324-132insCT
|
NP_003313.3:n.1324-133_1324-132insCT
|
|
NM_003322.6:c.1324-133_1324-132insCT
MANE Select
|
NP_003313.3:n.1324-133_1324-132insCT
|
|
NM_001289395.2:c.1165-133_1165-132insCT
|
NP_001276324.1:n.1165-133_1165-132insCT
|
|