ENST00000256925.12:c.845+4402G>T
MANE Select
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ENSP00000256925.7:n.845+4402G>T
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ENST00000256925.11:c.845+4402G>T
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ENSP00000256925.7:n.845+4402G>T
|
|
ENST00000400473.6:c.-137+6339G>T
|
ENSP00000383321.2:n.-137+6339G>T
|
|
ENST00000578052.1:n.59+4402G>T
|
|
|
ENST00000579963.5:c.-137+6358G>T
|
ENSP00000464435.1:n.-137+6358G>T
|
|
ENST00000580153.5:c.-137+4402G>T
|
ENSP00000461994.1:n.-137+4402G>T
|
|
ENST00000580644.5:n.115+4402G>T
|
|
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ENST00000582882.5:c.184+4402G>T
|
|
|
ENST00000583220.5:n.149+4402G>T
|
|
|
NM_001100619.2:c.845+4402G>T
|
NP_001094089.1:n.845+4402G>T
|
|
NM_001256438.1:c.-137+6339G>T
|
NP_001243367.1:n.-137+6339G>T
|
|
NR_023359.1:n.88+6358G>T
|
|
|
NR_023359.2:n.88+6358G>T
|
|
|
NM_001100619.3:c.845+4402G>T
MANE Select
|
NP_001094089.1:n.845+4402G>T
|
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