ENST00000455537.7:c.2938G>C
MANE Select
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ENSP00000408979.2:p.Ala980Pro
|
|
ENST00000674619.1:c.2959G>C
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ENSP00000502270.1:p.Ala987Pro
|
|
ENST00000675697.1:c.29G>C
|
|
|
ENST00000675737.1:n.342G>C
|
|
|
ENST00000675882.1:n.2461G>C
|
|
|
ENST00000675929.1:n.1496G>C
|
|
|
ENST00000676055.1:c.29G>C
|
|
|
ENST00000676457.1:c.2833G>C
|
ENSP00000501588.1:p.Ala945Pro
|
|
ENST00000286452.5:c.2671G>C
|
ENSP00000286452.5:p.Ala891Pro
|
|
ENST00000455537.6:c.2938G>C
|
ENSP00000408979.2:p.Ala980Pro
|
|
ENST00000552227.1:n.221G>C
|
|
|
NM_004984.2:c.2938G>C
|
NP_004975.2:p.Ala980Pro
|
|
NM_001354705.1:c.2671G>C
|
NP_001341634.1:p.Ala891Pro
|
|
NM_004984.3:c.2938G>C
|
NP_004975.2:p.Ala980Pro
|
|
XR_002957324.1:n.3171G>C
|
|
|
NM_004984.4:c.2938G>C
MANE Select
|
NP_004975.2:p.Ala980Pro
|
|
NM_001354705.2:c.2671G>C
|
NP_001341634.1:p.Ala891Pro
|
|