ENST00000389048.8:c.3572C>A
MANE Select
|
ENSP00000373700.3:p.Pro1191His
|
|
ENST00000431873.6:c.799C>A
|
|
|
ENST00000638605.1:n.449C>A
|
|
|
ENST00000642122.1:c.368C>A
|
ENSP00000493203.1:p.Pro123His
|
|
ENST00000389048.7:c.3572C>A
|
ENSP00000373700.3:p.Pro1191His
|
|
ENST00000431873.5:c.452C>A
|
ENSP00000414027.2:p.Pro151His
|
|
ENST00000618119.4:c.2441C>A
|
ENSP00000482733.1:p.Pro814His
|
|
NM_004304.4:c.3572C>A
|
NP_004295.2:p.Pro1191His
|
|
NM_001353765.1:c.368C>A
|
NP_001340694.1:p.Pro123His
|
|
XM_024452778.1:c.725C>A
|
XP_024308546.1:p.Pro242His
|
|
XM_024452779.1:c.368C>A
|
XP_024308547.1:p.Pro123His
|
|
NM_004304.5:c.3572C>A
MANE Select
|
NP_004295.2:p.Pro1191His
|
|
NM_001353765.2:c.368C>A
|
NP_001340694.1:p.Pro123His
|
|