ENST00000367412.2:c.1344T>C
MANE Select
|
ENSP00000356382.2:p.Pro448=
|
|
ENST00000649282.1:c.99T>C
|
ENSP00000497116.1:p.Pro33=
|
|
ENST00000367412.1:c.1344T>C
|
ENSP00000356382.1:p.Pro448=
|
|
NM_001994.2:c.1344T>C , LRG_550t1:c.1344T>C
|
NP_001985.2:p.Pro448=
|
|
XM_011509283.1:c.1344T>C
|
XP_011507585.1:p.Pro448=
|
|
XM_011509284.1:c.1341T>C
|
XP_011507586.1:p.Pro447=
|
|
XM_011509285.1:c.1248T>C
|
XP_011507587.1:p.Pro416=
|
|
XM_011509286.1:c.1200T>C
|
XP_011507588.1:p.Pro400=
|
|
XM_011509283.2:c.1344T>C
|
XP_011507585.1:p.Pro448=
|
|
XM_011509284.2:c.1341T>C
|
XP_011507586.1:p.Pro447=
|
|
XM_011509286.2:c.1200T>C
|
XP_011507588.1:p.Pro400=
|
|
NM_001994.3:c.1344T>C
MANE Select
|
NP_001985.2:p.Pro448=
|
|