ENST00000644971.2:c.8845C>A
MANE Select
|
ENSP00000496448.1:p.Pro2949Thr
|
|
ENST00000647633.1:c.9586C>A
|
ENSP00000497649.1:p.Pro3196Thr
|
|
ENST00000375244.7:c.8845C>A
|
ENSP00000364393.3:p.Pro2949Thr
|
|
ENST00000611016.2:c.1999C>A
|
ENSP00000483409.1:p.Pro667Thr
|
|
NM_019105.6:c.8839C>A
|
NP_061978.6:p.Pro2947Thr
|
|
NM_001365276.1:c.8845C>A
|
NP_001352205.1:p.Pro2949Thr
|
|
NM_019105.7:c.8839C>A
|
NP_061978.6:p.Pro2947Thr
|
|
NM_001365276.2:c.8845C>A
MANE Select
|
NP_001352205.1:p.Pro2949Thr
|
|
NM_019105.8:c.8839C>A
|
NP_061978.6:p.Pro2947Thr
|
|