ENST00000586569.3:c.512C>A
MANE Select
|
ENSP00000465500.1:p.Pro171His
|
|
ENST00000639222.1:c.512C>A
|
ENSP00000492422.1:p.Pro171His
|
|
ENST00000269485.11:c.512C>A
|
ENSP00000269485.7:p.Pro171His
|
|
ENST00000586569.2:c.512C>A
|
ENSP00000465500.1:p.Pro171His
|
|
ENST00000587697.1:n.430C>A
|
|
|
ENST00000616710.4:c.512C>A
|
ENSP00000479567.1:p.Pro171His
|
|
ENST00000617039.4:c.512C>A
|
ENSP00000482466.1:p.Pro171His
|
|
NM_001270949.1:c.512C>A
|
NP_001257878.1:p.Pro171His
|
|
NM_001270950.1:c.512C>A
|
NP_001257879.1:p.Pro171His
|
|
NM_001270951.1:c.512C>A
|
NP_001257880.1:p.Pro171His
|
|
NM_001278268.1:c.470C>A
|
NP_001265197.1:p.Pro157His
|
|
NM_003839.3:c.512C>A
|
NP_003830.1:p.Pro171His
|
|
XM_011526244.1:c.527C>A
|
XP_011524546.1:p.Pro176His
|
|
XM_011526245.1:c.404C>A
|
XP_011524547.1:p.Pro135His
|
|
XR_935263.1:n.542C>A
|
|
|
XM_011526244.2:c.527C>A
|
XP_011524546.1:p.Pro176His
|
|
XM_011526245.2:c.404C>A
|
XP_011524547.1:p.Pro135His
|
|
XM_017026064.1:c.404C>A
|
XP_016881553.1:p.Pro135His
|
|
XM_017026065.1:c.362C>A
|
XP_016881554.1:p.Pro121His
|
|
XM_017026066.1:c.302C>A
|
XP_016881555.1:p.Pro101His
|
|
NM_003839.4:c.512C>A
MANE Select
|
NP_003830.1:p.Pro171His
|
|
NM_001270951.2:c.512C>A
|
NP_001257880.1:p.Pro171His
|
|
NM_001278268.2:c.470C>A
|
NP_001265197.1:p.Pro157His
|
|
NM_001270949.2:c.512C>A
|
NP_001257878.1:p.Pro171His
|
|
NM_001270950.2:c.512C>A
|
NP_001257879.1:p.Pro171His
|
|