ENST00000322213.9:c.1740T>G
MANE Select
|
ENSP00000323421.3:p.Pro580=
|
|
ENST00000674590.1:c.972T>G
|
ENSP00000502626.1:p.Pro324=
|
|
ENST00000675065.1:n.1092T>G
|
|
|
ENST00000675504.1:c.1674T>G
|
ENSP00000502524.1:p.Pro558=
|
|
ENST00000322213.8:c.1740T>G
|
ENSP00000323421.3:p.Pro580=
|
|
ENST00000375340.10:c.1674T>G
|
ENSP00000364489.7:p.Pro558=
|
|
NM_001281463.1:c.1674T>G , LRG_773t1:c.1674T>G
|
NP_001268392.1:p.Pro558=
|
|
NM_006306.3:c.1740T>G , LRG_773t2:c.1740T>G
|
NP_006297.2:p.Pro580=
|
|
NM_006306.4:c.1740T>G
MANE Select
|
NP_006297.2:p.Pro580=
|
|