ENST00000411466.7:c.7339C>G
|
ENSP00000405186.3:p.Pro2447Ala
|
|
ENST00000704023.1:c.1593+26C>G
|
|
|
ENST00000706321.1:c.7339C>G
|
ENSP00000516346.1:p.Pro2447Ala
|
|
ENST00000262518.9:c.7339C>G
MANE Select
|
ENSP00000262518.4:p.Pro2447Ala
|
|
ENST00000262518.8:c.7339C>G
|
ENSP00000262518.4:p.Pro2447Ala
|
|
ENST00000380361.7:c.6808C>G
|
ENSP00000369719.3:p.Pro2270Ala
|
|
ENST00000395059.6:c.6562C>G
|
ENSP00000378499.3:p.Pro2188Ala
|
|
NM_006662.2:c.7339C>G
|
NP_006653.2:p.Pro2447Ala
|
|
NM_006662.3:c.7339C>G
MANE Select
|
NP_006653.2:p.Pro2447Ala
|
|