ENST00000229771.11:c.1353G>C
MANE Select
|
ENSP00000229771.6:p.Gln451His
|
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ENST00000229771.10:c.1353G>C
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ENSP00000229771.6:p.Gln451His
|
|
ENST00000322263.8:c.1194G>C
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ENSP00000319414.4:p.Gln398His
|
|
ENST00000495781.1:n.529G>C
|
|
|
ENST00000614066.4:c.1347G>C
|
ENSP00000477534.1:p.Gln449His
|
|
NM_001289395.1:c.1194G>C
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NP_001276324.1:p.Gln398His
|
|
NM_003322.4:c.1353G>C
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NP_003313.3:p.Gln451His
|
|
NM_003322.5:c.1353G>C
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NP_003313.3:p.Gln451His
|
|
NM_003322.6:c.1353G>C
MANE Select
|
NP_003313.3:p.Gln451His
|
|
NM_001289395.2:c.1194G>C
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NP_001276324.1:p.Gln398His
|
|