ENST00000399503.4:c.3101C>A
MANE Select
|
ENSP00000382423.3:p.Pro1034His
|
|
ENST00000399503.3:c.3101C>A
|
ENSP00000382423.3:p.Pro1034His
|
|
NM_005921.1:c.3101C>A
|
NP_005912.1:p.Pro1034His
|
|
XM_005248519.3:c.2723C>A
|
XP_005248576.2:p.Pro908His
|
|
XM_011543406.1:c.2846C>A
|
XP_011541708.1:p.Pro949His
|
|
XM_011543407.1:c.2822C>A
|
XP_011541709.1:p.Pro941His
|
|
XM_011543408.1:c.3101C>A
|
XP_011541710.1:p.Pro1034His
|
|
XM_017009484.1:c.2690C>A
|
XP_016864973.1:p.Pro897His
|
|
XM_017009485.1:c.2612C>A
|
XP_016864974.1:p.Pro871His
|
|
XR_001742068.2:n.3132C>A
|
|
|
NM_005921.2:c.3101C>A
MANE Select
|
NP_005912.1:p.Pro1034His
|
|