ENST00000367412.2:c.1337C>A
MANE Select
|
ENSP00000356382.2:p.Ser446Tyr
|
|
ENST00000649282.1:c.92C>A
|
ENSP00000497116.1:p.Ser31Tyr
|
|
ENST00000367412.1:c.1337C>A
|
ENSP00000356382.1:p.Ser446Tyr
|
|
NM_001994.2:c.1337C>A , LRG_550t1:c.1337C>A
|
NP_001985.2:p.Ser446Tyr
|
|
XM_011509283.1:c.1337C>A
|
XP_011507585.1:p.Ser446Tyr
|
|
XM_011509284.1:c.1334C>A
|
XP_011507586.1:p.Ser445Tyr
|
|
XM_011509285.1:c.1241C>A
|
XP_011507587.1:p.Ser414Tyr
|
|
XM_011509286.1:c.1193C>A
|
XP_011507588.1:p.Ser398Tyr
|
|
XM_011509283.2:c.1337C>A
|
XP_011507585.1:p.Ser446Tyr
|
|
XM_011509284.2:c.1334C>A
|
XP_011507586.1:p.Ser445Tyr
|
|
XM_011509286.2:c.1193C>A
|
XP_011507588.1:p.Ser398Tyr
|
|
NM_001994.3:c.1337C>A
MANE Select
|
NP_001985.2:p.Ser446Tyr
|
|